The Products of Animal Origin (Third Country Imports) (Wales) Regulations 2007

Welsh Statutory Instruments

2007 No. 376 (W.36)

AGRICULTURE, WALES

The Products of Animal Origin (Third Country Imports) (Wales) Regulations 2007

Made

13 February 2007

Coming into force

14 February 2007

The National Assembly for Wales is designated(1) for the purposes of section 2(2) of the European Communities Act 1972(2) in relation to the common agricultural policy of the European Community.

Exercising the powers conferred on it by that section save in relation to fees charged by the National Assembly, and, in relation to such fees, exercising the powers conferred on it by section 56(1) and (2) of the Finance Act 1973(3) and with the consent of the Treasury, it makes the following Regulations—

PART 1 Introduction

Title, application and commencement

1.—(1) The title of these Regulations is the Products of Animal Origin (Third Country Imports) (Wales) Regulations 2007.

(2) These Regulations apply in relation to Wales and come into force on 14 February 2007.

Interpretation

2.—(1) In these Regulations—

“the Agency” (“yr Asiantaeth”) means the Food Standards Agency;

“Article 9 product” (“cynnyrch Erthygl 9”)means a product from a third country which is first brought into the relevant territories at one border inspection post but is intended for import via another, as described (in relation to consignments) in Article 9(1) of Directive 97/78/EC, whether or not the product is transhipped or unloaded at the first border inspection post;

“authorised officer” (“swyddog awdurdodedig”) means a person who is authorised by the National Assembly, a local authority or the Agency, either generally or specially, to act in matters arising under these Regulations, whether or not he or she is an officer of the National Assembly or of a local authority or the Agency;

“border inspection post” (“safle arolygu ar y ffin”) means—

(a)

a border inspection post which is included in the list contained in the Annex to Decision 2001/881/EC; or

(b)

a border inspection post in the Republic of Iceland or the Kingdom of Norway which is included in the list contained in the Annex to Decision No. 86/02/COL of the EFTA Surveillance Authority(4);

“border inspection post of destination” (“safle arolygu ar y ffin ar gyfer cyrchfan”) means the border inspection post via which an Article 9 product is intended for import;

“border inspection post of introduction” (“safle arolygu ar y ffin ar gyfer cyflwyno”) means the border inspection post at which an Article 9 product is first brought into the relevant territories;

“carrier who has charge for the time being” (“cludydd sydd â gofal am y tro”) of a product, consignment or part consignment includes the driver of any vehicle, the pilot of any aircraft and the master of any vessel (but not the driver of any train) transporting the same;

“the Commissioners” (“y Comisiynwyr”) means the Commissioners for Her Majesty’s Revenue and Customs;

“common veterinary entry document” (“dogfen fynediad filfeddygol gyffredin”) means a document in the form set out in Annex III to Regulation (EC) No. 136/2004 (laying down procedures for veterinary checks at Community border inspection posts on products imported from third countries)(5);

“Community establishment of origin” (“sefydliad tarddiad Cymunedol”) means the premises located in a member State at which a returned product attained the form in which it was originally exported from the relevant territories;

“consignment” (“llwyth”) means a quantity of products of the same type covered by the same veterinary certificate or veterinary document, or other document provided for by veterinary legislation, conveyed by the same means of transport and coming from the same third country or part of a third country;

“the Customs Code” (“y Cod Tollau”) means Council Regulation (EEC) No. 2913/92 (establishing the Community Customs Code)(6);

“the customs territory of the Community” (“tiriogaeth dollau'r Gymuned”) has the same meaning as in Article 3 of the Customs Code;

“customs warehouse” (“warws dollau”) means a warehouse which fulfils the conditions of Articles 98 to 113 of the Customs Code, in which goods are stored subject to the customs warehousing procedure referred to in those Articles;

“Decision 2001/881/EC” (“Penderfyniad 2001/881/EC”) means Commission Decision 2001/881/EC (drawing up a list of border inspection posts agreed for veterinary checks on animals and animal products from third countries and updating the detailed rules concerning the checks to be carried out by the experts of the Commission)(7);

“destination establishment” (“sefydliad cyrchfan”), in relation to a product, means the establishment identified in the “delivery address” entry in Part 1 of the common veterinary entry document;

“Directive 97/78/EC” (“Cyfarwyddeb 97/78/EC”) means Council Directive 97/78/EC (laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries)(8);

“documentary check” (“gwiriad dogfennol”) means the examination of the veterinary certificates or veterinary documents or other documents accompanying a consignment, carried out in accordance with Article 4(3) of Directive 97/78/EC and Annex I to Regulation (EC) No. 136/2004;

“fishery products” (“cynhyrchion pysgodfeydd”) means all wild or farmed seawater and freshwater animals, whether or not live, and all edible forms, parts and products of such animals, including—

(a)

aquaculture animals and aquaculture products as defined in Article 2 of Council Directive 91/67/EEC (concerning the animal health conditions governing the placing on the market of aquaculture animals and products)(9);

(b)

filter-feeding lamellibranch molluscs; and

(c)

echinoderms, tunicates and marine gastropods intended for human consumption,

but excludes aquatic mammals, reptiles and frogs, and parts of those animals;

“free warehouse” (“warws rydd”) and “free zone” (“parth rhydd”) have the same meanings as in Title IV, Chapter 3, Section 1 of the Customs Code;

“identity check” (“gwiriad adnabod”) means a check by visual inspection to ensure that the veterinary certificates or veterinary documents or other documents accompanying a consignment tally with the products comprised in the consignment, carried out in accordance with Article 4(4)(a) of Directive 97/78/EC;

“import” (“mewnforio”), as a noun, means release for free circulation within the meaning of Article 79 of the Customs Code;

“import conditions” (“amodau mewnforio”) in relation to a product, means—

(a)

the conditions laid down for the import of that product in any Directive, Decision or Regulation listed in Schedule 1, including—

(i)

specific requirements laid down for the import of that product into a particular member State or a particular area of a member State; and

(ii)

conditions laid down for the import of that product for specific purposes;

(b)

the conditions laid down for the import of that product in any Decision listed in Schedule 2;

(c)

the conditions as to the country of origin of the product as laid down in any list of the third countries or parts of third countries from which imports of specified products are permitted and drawn up under paragraph 1 of Article 11 of Regulation (EC) No. 854/2004; and

(d)

the conditions as to the establishment of origin of the product as laid down in any list of establishments from which imports of specified products are permitted and drawn up under paragraph 1 of Article 12 of Regulation (EC) No. 854/2004 (laying down specific rules for the organisation of official controls on products of animal origin intended for human consumption)(10);

“local authority” (“awdurdod lleol”) means—

(a)

where there is a port health authority, that port health authority;

(b)

where there is no port health authority, the council of the county or county borough as the case may be;

“National Assembly” (“Cynulliad Cenedlaethol”) means the National Assembly for Wales of Cathays Park, Cardiff CF10 3NQ;

“non-conforming product” (“cynnyrch nad yw'n cydymffurfio”) means a product which does not comply with the import conditions;

“official fish inspector” (“arolygydd pysgod swyddogol”) means an environmental health officer appointed as an official fish inspector by a local authority under regulation 6(2)(b);

“official veterinary surgeon” (“milfeddyg swyddogol”) means a veterinary surgeon who is appointed by the National Assembly under regulation 6(1)(a) or by a local authority under regulation 6(2)(a);

“operator” (“gweithredydd”) means—

(a)

in relation to a border inspection post, the person who provides premises and other facilities for the carrying out of veterinary checks at that border inspection post; and

(b)

in relation to a Community establishment of origin or a destination establishment, the person who occupies the same for the purposes of his or her business;

“owner” (“perchennog”), in relation to a product, consignment or part consignment, means the person in whom the property in the product, consignment or part is for the time being vested;

“part consignment” (“rhanlwyth”) means a consignment which has been split up into parts in accordance with Article 5 of Regulation (EC) No. 136/2004;

“person appearing to have charge” (“person y mae'n ymddangos ei fod â gofal”), in relation to a product, consignment, or part consignment, means any person, including a carrier, who appears to have possession, custody or control of the product, consignment or part consignment;

“person responsible for” (“person sy'n gyfrifol dros”), in relation to a product, consignment, or part consignment, is construed in accordance with regulation 3;

“physical check” (“gwiriad ffisegol”) means a check on a product (which may include checks on packaging and temperature and also sampling and laboratory testing) carried out in accordance with Article 4(4)(b) of, and Annex III to, Directive 97/78/EC and, in the case of laboratory testing, Annex II to Regulation (EC) No. 136/2004;

“premises” (“mangre”) includes any construction, installation, container or means of transport;

“product” (“cynnyrch”) means—

(a)

any product of animal origin listed in the Annex to Commission Decision 2002/349/EC (laying down the list of products to be examined at border inspection posts under Council Directive 97/78/EC)(11);

(b)

any grass, clover, lucerne or sainfoin which has been dried either naturally or artificially, and any product which is obtained by so drying any grass, clover, lucerne or sainfoin; and

(c)

any green cereal which has been dried either naturally or artificially, and any product (other than grain) which is obtained by drying any green cereal,

but does not include composite food products as specified in Article 3 of Commission Decision 2002/349/EC;

“Regulation (EC) No. 1774/2002” (“Rheoliad (EC) Rhif 1774/2002”) means Regulation (EC) No. 1774/2002 of the European Parliament and of the Council (laying down health rules concerning animal by-products not intended for human consumption)(12);

“Regulation (EC) No. 136/2004” (“Rheoliad (EC) Rhif 136/2004”) means Commission Regulation (EC) No. 136/2004 (laying down procedures for veterinary checks at Community border inspection posts on products imported from third countries)(13);

“the regulatory functions” (“y swyddogaethau rheoliadol”) means the functions assigned by these Regulations to authorised officers, official veterinary surgeons, official fish inspectors and assistants appointed under regulation 6;

“relevant document” (“dogfen berthnasol”) means any required document and any commercial or other certificate or document relating to a product, including the manifest of any sea-going vessel or aircraft;

“the relevant territories” (“y tiriogaethau perthnasol”) means an area comprising the territories of the member States, as listed in Annex I to Directive 97/78/EC, the Republic of Iceland, the Kingdom of Norway (except Svalbard), the Principality of Andorra, the Faroe Islands and the Republic of San Marino;

“required document” (“dogfen ofynnol”) means any original veterinary certificate, original veterinary document or other original document required in relation to a product by virtue of any Directive, Decision or Regulation listed in Schedule 1;

“returned product” (“cynnyrch a ddychwelwyd”) means a product originally exported from the customs territory of the Community which is returned there because it has been refused by a third country;

“ships' store” (“storfa longau”) means closed premises referred to in Article 13(1)(c), or a specially approved warehouse referred to in Article 13(2)(a), of Directive 97/78/EC;

“third country” (“trydydd wlad”) means a country not comprised in the relevant territories;

“transhipped product” (“cynnyrch a drawslwythwyd”) means an Article 9 product which is transhipped or unloaded in the way described (in relation to consignments) in Article 9(1) of Directive 97/78/EC at its border post of introduction;

“transit” (“tramwy”) means transit from one third country to another, passing through one or more member States, under the external transit procedure referred to in Articles 91 to 97 of the Customs Code;

“transit product” (“cynnyrch tramwy”) means a product originating in a third country which, according to the information forwarded in advance referred to in Article 3(3) of Directive 97/78/EC, will undergo transit; and

“veterinary check” (“gwiriad milfeddygol”) means any check provided for in Directive 97/78/EC including a documentary check, an identity check or a physical check.

(2) Products brought into Wales from the Republic of Iceland, other than fishery products, are regarded for the purposes of these Regulations as products brought in from a third country.

(3) Subject to paragraph (4), for the purposes of these Regulations, a person brings a product into a territory or area if—

(a) he or she brings it into that territory or area as its owner;

(b) he or she brings it into that territory or area as a carrier; or

(c) a carrier brings it into that territory or area on that person’s instructions.

(4) A product on board a means of transport operating internationally which is intended for consumption by the crew or passengers of that means of transport is not brought into a territory or area if—

(a) the product is not unloaded; or

(b) it is transferred directly from one means of transport operating internationally to another at the same port or airport and under supervision, within the meaning of Article 4(13) of the Customs Code, by the Commissioners.

(5) Any reference in these Regulations to a Community instrument is a reference to that instrument as amended from time to time.

Person responsible for a consignment

3.—(1) In these Regulations, a reference to “person responsible for”, in relation to a product, consignment or part consignment is construed in accordance with the following paragraphs.

(2) Until—

(a) the product, consignment or part consignment first arrives at a border inspection post in Wales; or

(b) in the case of an Article 9 product, or a consignment or part consignment of Article 9 products, it arrives at a border inspection post of destination in Wales,

the person responsible for the product, consignment or part consignment is the person specified in paragraph (3).

(3) The person referred to in paragraph (2) is—

(a) the person referred to in Article 38(1) of the Customs Code who brings the product, consignment or part consignment into the customs territory of the Community;

(b) a person referred to in Article 38(2) of the Customs Code who assumes responsibility for the carriage of the product, consignment or part consignment after it has been brought into the customs territory of the Community; or

(c) a person in whose name the persons referred to in sub-paragraph (a) or (b) acted.

(4) From the time—

(a) the product, consignment or part consignment first arrives at a border inspection post in Wales until it leaves that border inspection post; or

(b) in the case of an Article 9 product, or a consignment or part consignment of Article 9 products, it arrives at a border inspection post of destination in Wales until it leaves that border inspection post of destination,

the person responsible for the product, consignment or part consignment is the person specified in paragraph (5).

(5) The person referred to in paragraph (4) is—

(a) the person in whose name the persons referred to in paragraph (3)(a) or (b) acted;

(b) if the product, consignment or part consignment is in temporary storage, as referred to in Article 50 of the Customs Code, the person referred to in Article 51(2) of the Customs Code who holds it in temporary storage; or

(c) if—

(i) a person referred to in sub-paragraph (a) or (b), has appointed a representative in his or her dealings with the customs authorities, within the meaning of Article 5 of the Customs Code, and

(ii) the representative is given or assumes responsibility for ensuring that the product, consignment or part consignment undergoes veterinary checks,

that representative.

(6) After—

(a) the product, consignment or part consignment leaves a border inspection post referred to in paragraph (4)(a); or

(b) in the case of an Article 9 product, or a consignment or part consignment of Article 9 products, it leaves the border inspection post of destination,

the person responsible for the product, consignment or part consignment is the person specified in paragraph (7).

(7) The person referred to in paragraph (6) is—

(a) the person who made a customs declaration, within the meaning of Article 64 of the Customs Code, covering the product, consignment or part consignment; or

(b) if no such customs declaration has been made, the person capable of making it.

Exemption for authorised products and personal imports

4.—(1) Parts 3 to 9 do not apply to products brought into Wales from a third country with the previous authorisation of the National Assembly as trade samples, for exhibition, or for particular studies or analyses.

(2) The National Assembly’s authorisation—

(a) must be in writing;

(b) must in the case of products brought in—

(i) as trade samples or for exhibition, be made subject to a condition that they must not be marketed; and

(ii) for particular studies or analyses, be made subject to a condition that they must not be supplied for human consumption;

(c) may be made subject to such other conditions (if any) as it considers necessary for the protection of public or animal health; and

(d) may be amended, suspended or revoked in writing at any time.

(3) No person may—

(a) use a product to which the exemption in paragraph (1) applies for any purpose for which it has not been authorised, or contravene any condition referred to in paragraph (2)(b); or

(b) contravene any other condition of the National Assembly’s authorisation in relation to such a product.

(4) In the case of products brought in for exhibition or studies and any quantities of products brought in for analyses that remain following those analyses, the person who brought them in must as soon as possible when the exhibition, studies or analyses have finished, and in accordance with any conditions specified in the National Assembly’s authorisation—

(a) redispatch them to a third country; or

(b) dispose of them in accordance with Regulation (EC) No. 1774/2002 and the Animal By-Products (Wales) Regulations 2006(14).

(5) Where an authorised officer considers that there has been a breach of paragraph (3)(a) or (4) in relation to a product, he or she must by notice in writing served on the person appearing to have charge of that product, take charge of it and either—

(a) redispatch it to a destination, agreed with the person who brought it in, located in a third country within a period of sixty days commencing with the day following the service of the notice; or

(b) dispose of it as if it were Category 1 material under Regulation (EC) No. 1774/2002 in the facilities provided for that purpose nearest to the place at which the authorised officer takes charge of it.

(6) Where an authorised officer considers that there has been a breach of paragraph (3)(b) in relation to a product, he or she may by notice in writing served on the person appearing to have charge of that product, take charge of it and take either of the steps specified in paragraph (5)(a) and (b).

(7) Part 3, with the exception of regulation 25, and Parts 4 to 9 do not apply to-—

(a) powdered infant milk, infant food, or special foods required for medical reasons containing meat, meat products, milk or milk products from a third country if—

(i) they form part of a traveller’s personal luggage and are intended for his or her personal consumption or use;

(ii) they do not exceed in quantity that which could reasonably be consumed by an individual;

(iii) they do not require refrigeration before opening;

(iv) they are packaged proprietary brand products for direct sale to the final consumer; and

(v) their packaging is unbroken, unless they are in current use;

(b) meat, meat products, milk or milk products from the Faroe Islands, Greenland, the Republic of Iceland, Liechtenstein, or Switzerland if—

(i) they form part of a traveller’s personal luggage, or are sent by post or carrier (otherwise than by way of trade or as a trade sample) and are addressed to a private individual in Wales;

(ii) they are intended for the personal consumption of the traveller or the addressee, as the case may be; and

(iii) their combined total weight in any traveller’s personal luggage or in any consignment sent by post or carrier to a private individual does not exceed 5 kilograms; or

(c) products in the personal luggage of a traveller if they are intended for his or her personal consumption or which are sent by post or carrier (otherwise than by way of trade or as a trade sample) and addressed to a private individual in Wales, if they are intended for his or her personal consumption, and if they—

(i) are not meat, meat products, milk or milk products;

(ii) do not exceed one kilogram in weight;

(iii) come from a third country or part of a third country from which their importation is permitted in accordance with a list drawn up by an instrument in Schedule 1; and

(iv) do not come from a third country or part of a third country from which their importation is prohibited by any instrument in Schedule 1.

(8) In this regulation “meat” (“cig”), “meat products” (“cynhyrchion cig”), “milk” (“llaeth”) and “milk products” (“cynhyrchion llaeth”) mean products of those types listed in sections 01 — 04 under the heading I.2, Title I in the Annex to Commission Decision 2002/349/EC.

PART 2 Enforcement

Enforcement authorities and exchange of information

5.—(1) These Regulations must be enforced—

(a) by the National Assembly at a border inspection post solely designated and approved for veterinary checks on products referred to in Regulation (EC) No. 1774/2002;

(b) by the Agency at—

(i) any cutting plant, game-handling establishment or slaughterhouse; and

(ii) premises at which the Agency enforces the Food Hygiene (Wales) Regulations 2006(15) by virtue of regulation 5(2)(b) of those Regulations;

(c) subject to paragraph (2), by each local authority within its area, including at any border inspection post in that area, except at a border inspection post referred to in sub-paragraph (a) and at premises referred to in sub-paragraph (b).

(2) At points of entry, regulation 16 must be enforced by the Commissioners and not the local authority.

(3) In cases where an officer of a local authority, when exercising any statutory function, discovers at a point of entry a consignment or product that he or she considers may have been brought in breach of regulation 16, he or she must notify an officer of Revenue and Customs and detain the consignment or product until an officer of Revenue and Customs takes charge of it.

(4) In cases where an officer of a local authority who is not an authorised officer for the purposes of these Regulations, when exercising any statutory function, discovers at any place other than a point of entry or a border inspection post, a consignment or product —

(a) in relation to which he or she considers these Regulations may not have been complied with; or

(b) that he or she considers is from a third country and may present a risk to animal or public health,

he or she must notify an authorised officer and detain the consignment or product until an authorised officer takes charge of it.

(5) If the National Assembly considers that a local authority is failing or has failed to enforce these Regulations generally, or in any class of cases, or in an individual case, it may empower an authorised officer or the Agency to enforce them in place of that local authority.

(6) The National Assembly or the Agency may recover from the local authority concerned any expenses reasonably incurred by it under paragraph (5).

(7) The National Assembly, the Commissioners, any local authority and the Agency may exchange information for the purposes of these Regulations, and may divulge information to the enforcement authorities in England, Scotland and Northern Ireland for the purposes of these Regulations or the equivalent Regulations in those jurisdictions.

(8) Paragraph (7) is without prejudice to any other power of the National Assembly, the Commissioners, any local authority and the Agency to disclose information.

(9) No person, including a servant of the Crown, may disclose any information received from the Commissioners under paragraph (7) if—

(a) the information relates to a person whose identity—

(i) is specified in the disclosure; or

(ii) can be deduced from the disclosure;

(b) the disclosure is for a purpose other than the purposes specified in paragraph (7); and

(c) the Commissioners have not given their prior consent to the disclosure.

(10) In paragraph (1), the terms “cutting plant” (“safle torri”), “game-handling establishment” (“sefydliad trin anifeiliaid hela”) and “slaughterhouse” (“lladd-dy”) have the meaning that they bear in regulation 5(6) of the Food Hygiene (Wales) Regulations 2006.

(11) In this regulation, “point of entry” (“pwynt mynediad”) means any place where goods are subject to customs supervision under Articles 37 and 38 of the Customs Code, other than a border inspection post.

Appointment of official veterinary surgeons and official fish inspectors

6.—(1) The National Assembly must appoint—

(a) such veterinary surgeons who have participated in a special training programme referred to in Article 27 of Directive 97/78/EC to carry out the regulatory functions at any border inspection post solely designated and approved for veterinary checks on products referred to in Regulation (EC) No. 1774/2002; and

(b) such appropriately trained assistants for each veterinary surgeon appointed under sub-paragraph (a),

as may be necessary for the proper performance of the regulatory functions.

(2) A local authority must appoint—

(a) such veterinary surgeons who have participated in a special training programme referred to in Article 27 of Directive 97/78/EC to carry out the regulatory functions at each border inspection post in its area, other than a border inspection post referred to in paragraph (1)(a);

(b) such environmental health officers to be official fish inspectors to carry out the regulatory functions in relation to fishery products at each border inspection post in its area, other than a border inspection post referred to in paragraph (1)(a); and

(c) such appropriately trained assistants for each official veterinary surgeon appointed under paragraph (2)(a), and each official fish inspector appointed under paragraph (2)(b),

as may be necessary for the proper performance of the regulatory functions.

Exercise of enforcement powers

7.—(1) An official veterinary surgeon, an official fish inspector or an authorised officer may, at all reasonable hours and on producing, if so required, some duly authenticated document showing his or her authority, exercise the powers conferred by regulations 8 and 9 for the purpose of—

(a) enforcing these Regulations;

(b) enforcing any declaration made by the National Assembly or the Agency under regulation 61;

(c) ascertaining whether these Regulations are being or have been complied with; or

(d) verifying the identity, origin or destination of any product.

(2) In the case of an official veterinary surgeon, an official fish inspector or an authorised officer appointed or authorised by a local authority, the powers conferred by regulations 8 and 9 must be exercised—

(a) within the area of that local authority, and

(b) outside the area of that local authority for the purpose of ascertaining whether these Regulations are being or have been complied with within that area.

Powers of entry and inspection

8.—(1) An official veterinary surgeon, official fish inspector or authorised officer may—

(a) enter any border inspection post or other land or premises and inspect the same and anything in or on it, but admission to any premises used only as a dwelling-house must not be demanded as of right unless 24 hours' written notice of the intended entry has been given to the occupier;

(b) open any bundle, package, packing case, or item of personal luggage, or require any person in possession of or accompanying the same to open it;

(c) inspect the contents of any bundle, package, packing case or item of personal luggage opened under sub-paragraph (b);

(d) inspect any product, including its packaging, seals, marking, labelling and presentation, and any plant or equipment used for or in connection with any product;

(e) take samples of any product for laboratory tests, for checking against any relevant document relating to the product or otherwise for checking compliance with the import conditions.

(2) Where an official veterinary surgeon, official fish inspector or authorised officer—

(a) has carried out any of the activities listed in paragraph (1); and

(b) is satisfied that further checks need to be carried out,

he or she may serve a notice in writing on the person appearing to have charge of the consignment, requiring that the consignment or part consignment be stored under the supervision of the official veterinary surgeon, official fish inspector or authorised officer, as the case may be, at such place and under such conditions as he or she may direct in the notice, until he or she serves a further notice in writing that the same may be removed.

(3) The costs of the storage referred to in paragraph (2) must be paid by the person responsible for the consignment.

(4) An official veterinary surgeon, official fish inspector or authorised officer entering any land or premises under paragraph 1(a) may take with him or her other persons acting under his or her instructions and, unless he or she is entering premises used only as a dwelling house—

(a) a representative of the European Commission; and

(b) a representative of the authorities of a third country, appointed and acting in accordance with the provisions of one of the equivalence decisions listed in Schedule 2.

Powers in relation to documents

9.—(1) An official veterinary surgeon, official fish inspector or authorised officer may—

(a) require any person appearing to have charge of a product, any person responsible for a product and any corporate officer, employee, servant or agent of any such persons, to produce any relevant document in his or her possession or under his or her control relating to the product, and to supply such additional information in his or her possession or under his or her control relating to the product as the official veterinary surgeon, official fish inspector or authorised officer may reasonably request;

(b) examine any relevant document relating to a product and, where it is kept by means of a computer, have access to and inspect and check the operation of any computer and associated apparatus or material which is or has been used in connection with that relevant document;

(c) make and retain such copies as he or she may think fit of any relevant document relating to a product; and

(d) seize and retain any relevant document relating to a product which the official veterinary surgeon, official fish inspector or authorised officer has reason to believe may be required as evidence in proceedings under these Regulations, and, where any such relevant document is kept by means of a computer, require it to be produced in a form in which it may be taken away.

(2) In this regulation, “corporate officer” (“swyddog corfforaethol”), in relation to a body corporate, means a director, member of the committee of management, chief executive, manager, secretary or other similar officer of the body, or a person purporting to act in any such capacity.

Protection of officials acting in good faith

10.—(1) No authorised officer, official veterinary surgeon, official fish inspector, or assistant appointed under regulation 6 is personally liable in respect of any act done by him or her in the performance or purported performance of the regulatory functions within the scope of his or her employment, if he or she did that act in the honest and reasonable belief that his or her duty under these Regulations required or entitled him or her to do so.

(2) Paragraph (1) does not relieve the National Assembly, a local authority or the Agency from any liability in respect of acts of its officers.

Entry warrants

11.—(1) If a justice of the peace, on sworn information in writing, is satisfied that there is reasonable ground for entry into any land or premises by an official veterinary surgeon, official fish inspector or authorised officer under regulation 8 for any of the purposes specified in regulation 7 and either—

(a) that entry has been refused, or a refusal is reasonably expected, and the official veterinary surgeon, official fish inspector or authorised officer has given notice of his or her intention to apply for an entry warrant to the occupier; or

(b) a request for entry, or the giving of such a notice, would defeat the object of entry, or entry is urgently required, or the land or premises are unoccupied, or the occupier is temporarily absent, and it would defeat the object of entry to await his or her return,

the justice may by warrant signed by him or her, and valid for one month, authorise the official veterinary surgeon, official fish inspector or authorised officer to enter the land or premises, if need be by reasonable force.

(2) An official veterinary surgeon, official fish inspector or authorised officer leaving any unoccupied premises which he or she has entered by virtue of a warrant must leave them as effectively secured against unauthorised entry as he or she found them.

Local authority returns

12.—(1) For each border inspection post in its area, a local authority must submit to the National Assembly a return comprising—

(a) the total number of consignments checked, categorised by groups of products and by country of origin;

(b) a list of consignments of which samples were taken and the results of any test or analysis of each sample; and

(c) a list of consignments required to be redispatched or disposed of under regulation 21 by the official veterinary surgeon or official fish inspector, together with, in each case, their country of origin, establishment of origin (if known), a description of the product concerned and the reason for refusal.

(2) The National Assembly must determine how frequently the returns referred to in paragraph (1) are to be submitted and what period of time they are to cover.

Suspension of border inspection posts and inspection centres

13.—(1) This regulation applies if the National Assembly is satisfied that—

(a) the continued operation of a border inspection post presents a serious risk to public or animal health; or

(b) at a border inspection post, there has been a serious breach of the requirements for the approval of border inspection posts laid down in Annex II to Directive 97/78/EC or in Commission Decision 2001/812/EC (laying down requirements for the approval of border inspection posts responsible for veterinary checks on products brought into the Community from third countries)(16).

(2) For the purposes of this regulation and any notice served under it, “approval” (“cymeradwyaeth”), in relation to a border inspection post or an inspection centre, means the approval of the border inspection post or inspection centre, as the case may be, in accordance with Article 6(2) or 6(4) of Directive 97/78/EC.

(3) Where this regulation applies, the National Assembly must suspend the border inspection post’s approval either in full or in part in accordance with paragraph (4), (5) or (6).

(4) The National Assembly may suspend the border inspection post’s approval in full by service—

(a) on the operator of the border inspection post; or

(b) where the border inspection post consists of more than one inspection centre, on the operator of each inspection centre (if they are different),

of a written notice stating that the approval of the premises as a border inspection post is suspended.

(5) If the National Assembly is satisfied that the serious risk to public or animal health referred to in paragraph (1)(a) or the serious breach of the requirements referred to in paragraph (1)(b) arises only in connection with one or more (but not all) of the categories of products for which the border inspection post is approved (as specified in the Annex to Decision 2001/881/EC), it may suspend the border inspection post’s approval in relation to that category or those categories of products by service of a written notice—

(a) on the operator of the border inspection post; or

(b) where the category of products concerned is, or the categories of products are, handled by different inspection centres within the border inspection post, on the operator of each of those inspection centres (if they are different),

stating that the approval of the premises as a border inspection post is suspended for that category, or those categories, of products.

(6) If the National Assembly is satisfied that the serious risk to public or animal health referred to in paragraph (1)(a) or the serious breach of the requirements referred to in paragraph (1)(b) arises only in connection with one inspection centre within the border inspection post, it may suspend the approval of the inspection centre by service of a written notice on the operator of the inspection centre stating that the approval of the premises as an inspection centre is suspended.

(7) Upon service of a notice under—

(a) paragraph (4), the premises will cease to be a border inspection post or an inspection centre within a border inspection post (as the case may be) until they are again so approved in accordance with Article 6(2)(a) of Directive 97/78/EC;

(b) paragraph (5), the premises will cease to be a border inspection post or an inspection centre within a border inspection post (as the case may be) approved for that category, or those categories, of products until they are again so approved in accordance with Article 6(2)(a) of Directive 97/78/EC; and

(c) paragraph (6), the premises will cease to be approved as an inspection centre within a border inspection post, until they are again so approved in accordance with Article 6(2)(a) of Directive 97/78/EC.

(8) The provisions of paragraph (7) apply in the case of a suspension effected under this regulation notwithstanding that the Annex to Decision 2001/881/EC may not have been updated to reflect that suspension.

(9) In this regulation, “inspection centre” (“canolfan arolygu”) means a facility forming part of a border inspection post that is listed along with the name of the border inspection post itself in the Annex to Decision 2001/881/EC.

Regulatory functions of official fish inspectors

14.  In Parts 3 to 8, and Part 12, where a fishery product is concerned, the expression “official veterinary surgeon” must be construed as a reference to an official fish inspector.

PART 3 Provisions Applicable to Products in General

Prohibition of non-conforming products

15.  No person may bring a non-conforming product into Wales from a third country, or a non-conforming product originating in a third country into Wales from elsewhere in the relevant territories unless—

(a) it is a transit product;

(b) its destination establishment is a warehouse in a free zone, a free warehouse or a customs warehouse approved under Article 12(4)(b) of Directive 97/78/EC, or a ships' store complying with Article 13 of Directive 97/78/EC, located (in each case) outside the United Kingdom; or

(c) its destination establishment is a cross-border means of sea transport and it is intended to be delivered directly on board that means of sea transport for the purposes of consumption there by staff and passengers.

Prohibition of introduction of products except at border inspection posts

16.—(1) No product may be brought into Wales from a third country except at a border inspection post designated and approved for veterinary checks on that product.

(2) No Article 9 product, the border inspection post of introduction of which is outside the United Kingdom, and the border inspection post of destination of which is in Wales, may be brought into Wales except at a border inspection post designated and approved for veterinary checks on that product.

(3) For the purposes of the application of the Customs and Excise Management Act 1979(17) to products introduced in contravention of this regulation, the time of their introduction is the time of importation in accordance with section 5 of that Act.

Advance notice of introduction or presentation

17.—(1) No person may—

(a) bring a product or consignment into Wales from a third country; or

(b) bring into Wales an Article 9 product or consignment of Article 9 products whose border inspection post of destination is in Wales,

unless notice of its introduction has been given to the official veterinary surgeon at a border inspection post designated and approved for veterinary checks on that product or consignment and a copy of it has been sent to the office of the Commissioners responsible for the area in which that border inspection post is situated.

(2) Where the border inspection post of introduction and the border inspection post of destination of an Article 9 product or consignment of Article 9 products are both in Wales, no person may present the product or consignment to a border inspection post unless notice of its presentation has been given to the official veterinary surgeon at a border inspection post of destination designated and approved for veterinary checks on that product or consignment and a copy of it has been sent to the office of the Commissioners responsible for the area in which that border inspection post is situated.

(3) The notice referred to in paragraphs (1) and (2)—

(a) must be in the form set out as Part 1 of the common veterinary entry document;

(b) may be supplied in electronic form;

(c) must be in Welsh or English and also in an official language of the country of destination in the relevant territories referred to in the notice, if other than the United Kingdom;

(d) must arrive at the border inspection post before the product or consignment is unloaded from the means of transport that brought it to Wales; and

(e) in the case of a notice given to a border inspection post of destination, must specify what checks have been carried out at the border inspection post of introduction.

Presentation of products at border inspection posts

18.—(1) Any person responsible for a product which is brought into Wales from a third country, or for an Article 9 product whose border inspection post of destination is in Wales which is brought into Wales, must present the product and the required documents, or ensure that the same are presented, without delay to the official veterinary surgeon at the inspection facility of the border inspection post to which notice of the product’s introduction or presentation was given under regulation 17.

(2) Where the border inspection post of introduction of an Article 9 product is in the United Kingdom and its border inspection post of destination is in Wales, any person responsible for the product after its removal from the border inspection post of introduction must present the product and the required documents, or ensure that the same are presented, without delay to the official veterinary surgeon at the inspection facility of the border inspection post of destination to which notice of the product’s presentation was given under regulation 17.

(3) A person who presents a product, other than a transit product or a product to which Part 8 applies, under paragraph 18(1) or (2) must present the required documents relating to that product drawn up in Welsh or English.

(4) A person who, under paragraph 18(1) or (2), presents a transit product or a product to which Part 8 applies accompanied by a required document in a language other than Welsh or English, must present at the same time a translation of the required document into Welsh or English, authenticated as accurate by an appropriately qualified expert.

Veterinary checks and official controls

19.—(1) Subject, in the case of transhipped products, to regulation 38, any person required by virtue of regulation 18 to present a product and its required documents, or to ensure that the same are presented, to an official veterinary surgeon must permit the official veterinary surgeon, or an assistant appointed under regulation 6(1)(b) or 6(2)(c), to carry out on the product or the required documents, as the case may be—

(a) a documentary check;

(b) an identity check;

(c) subject to regulations 41, 46 and 52, a physical check, and

(d) the official controls referred to in Article 14(1) of Regulation (EC) No. 882/2004 of the European Parliament and of the Council on official controls performed to ensure the verification of compliance with feed and food law, animal health and animal welfare rules(18),

and must render the official veterinary surgeon or assistant such assistance as he or she may reasonably request to enable him or her to carry out any of the said checks and controls.

(2) Where a product is presented to an official veterinary surgeon under regulation 18, no person may remove it or cause it to be removed from the border inspection post at which it was presented until the official veterinary surgeon has authorised its removal by issuing Part 2 of the common veterinary entry document for the product or for the consignment or part consignment which includes the product.

(3) Where a sample of a product is taken in the course of a physical check, pending removal of the product under paragraph (2) the person responsible for the consignment which includes the product must store it under the supervision of the official veterinary surgeon at such a place and under such conditions as the official veterinary surgeon may direct and must pay the costs of such storage.

(4) Where a product has been placed under official detention under Article 18 or 19 of Regulation (EC) No. 882/2004, no person may remove it from its place of detention.

(5) Where a product has been placed under official detention under Article 19 of Regulation (EC) No. 882/2004 and the official veterinary surgeon—

(a) has served a notice on the person responsible for the product under Article 19(1) of that Regulation; or

(b) considers that product to be injurious to human or animal health under Article 19(2) of that Regulation,

the person responsible for the product must comply with the notice if sub-paragraph (a) applies, or cooperate with the official veterinary surgeon in the destruction or redispatch of the product if sub-paragraph (b) applies.

(6) Any person who is aggrieved by a decision on a consignment made under Article 19 of Regulation (EC) No. 882/2004 may appeal within one month of the decision to a magistrates' court by way of complaint for an order and the Magistrates' Court Act 1980(19) applies to the proceedings.

(7) Pending the determination of an appeal under paragraph (6), the person responsible for the product concerned must ensure that it is stored under the supervision of the official veterinary surgeon at such a place and under such conditions as he or she may direct by notice.

Common veterinary entry document to accompany consignment

20.—(1) The person responsible for a consignment or part consignment in respect of which Part 2 of the common veterinary entry document has been issued, and any carrier who has charge of it for the time being, must ensure that the common veterinary entry document accompanies the consignment or part consignment—

(a) in the case of a consignment or part consignment intended for import, and subject to regulation 37(3), until the consignment or part consignment first reaches, after import, premises where products are stored, processed, handled, bought or sold; and

(b) in all other cases until the consignment or part consignment is no longer subject to supervision by the customs authorities, within the meaning of Article 4(13) of the Customs Code.

(2) The person who occupies for the purposes of his or her business the premises referred to in paragraph (1)(a) must take possession of the common veterinary entry document referred to in paragraph (1) and retain the same at the premises for a period of one year commencing with the day following its arrival there.

Products which fail veterinary checks

21.—(1) This regulation is subject to regulation 22.

(2) Where, following a veterinary check at a border inspection post, the official veterinary surgeon there decides that—

(a) a product, other than an excepted product, is a non-conforming product; or

(b) there is some other irregularity in relation to a product;

the official veterinary surgeon must comply with paragraph (3).

(3) The official veterinary surgeon must serve a notice in writing on the person responsible for the product requiring him or her either—

(a) to redispatch the product by the mode of transport by which it was brought into Wales from the border inspection post to a destination, agreed with the official veterinary surgeon, located in a third country within a period of sixty days commencing with the day following the service of the notice; or

(b) to dispose of the product in accordance with Regulation (EC) No. 1774/2002 in the facilities provided for that purpose nearest to the border inspection post.

(4) Subject to paragraph (6), where, following a veterinary check on a product, other than an excepted product, located away from a border inspection post, an authorised officer decides that the product is a non-conforming product, the authorised officer must comply with paragraph (5).

(5) The authorised officer must serve a notice in writing on the person appearing to have charge of the product, requiring him or her either—

(a) to redispatch the product by the mode of transport by which it was introduced into Wales from the border inspection post referred to in the notice to a destination, agreed with the authorised officer, located in a third country within a period of sixty days commencing with the day following the service of the notice; or

(b) to dispose of the product in accordance with Regulation (EC) No. 1774/2002 in the facilities provided for that purpose nearest to the location of the product.

(6) The product must be disposed of in accordance with paragraph 3(b) or 5(b) where—

(a) its redispatch is precluded on animal or public health grounds by—

(i) the results of a veterinary check, or

(ii) any animal or public health requirement laid down in a Community instrument in force on the date on which these Regulations are made,

or is otherwise impossible;

(b) the sixty-day period referred to in paragraph (3)(a) or 5(a) has elapsed; or

(c) the person responsible for the product or, if paragraph (4) applies, the owner of the product, agrees immediately to its disposal.

(7) The person responsible for, or, if paragraph (4) applies, the owner of, a product in respect of which a notice has been served under paragraph (3) or (5) must ensure that the product is stored until redispatch or disposal under the supervision of the official veterinary surgeon or the authorised officer at such a place and under such conditions as he or she may direct in the notice.

(8) Any person who is aggrieved by a decision referred to in paragraph (2) or (4) may appeal within one month of the decision to a magistrates' court by way of complaint for an order and the Magistrates' Courts Act 1980 applies to the proceedings.

(9) Pending the determination of an appeal under paragraph (8), paragraph (7) applies to the storage of the product concerned.

(10) In this regulation—

(a) “excepted product” (“cynnyrch a eithriwyd”) means a transit product which fulfils the requirements of Part 7 or a product whose destination establishment is referred to in regulation 15(b) or 15(c);

(b) “other irregularity” (“afreoleidd-dra arall”), in relation to a product, means—

(i) its introduction into Wales from a third country, or its presentation to a border inspection post of destination in Wales, without notice given under regulation 17;

(ii) any false or misleading information contained in a notice given under regulation 17;

(iii) any false or misleading information given under regulation 45 or 51;

(iv) any error, omission or false or misleading information in a required document, and any discrepancy between a required document and—

(aa) the notice of the product’s introduction or presentation given under regulation 17;

(bb) the product itself; or

(cc) the seals, stamps, marks or labels on the product, on the consignment which includes the product or on the container holding the product or the consignment;

(v) any defect in the product rendering it unfit for the purpose for which, according to the required documents, it is intended;

(vi) any defect in the seals, stamps, marks or labels referred to in paragraph (10)(b)(iv)(cc), including, in the case of a packaged product, any contravention of the labelling requirements laid down for that product in any Directive, Decision or Regulation listed in Schedule 1;

(vii) in the case of a product intended for import, any indication in the required documents that the product does not comply with the import conditions; and

(viii) in the case of a non-conforming product which is a transit product, or a product whose destination establishment is referred to in regulation 15(b) or 15(c), any contravention of the requirements laid down for that non-conforming product in any Directive, Decision or Regulation listed in Schedule 1.

Treatment as animal by-products

22.—(1) If the official veterinary surgeon or authorised officer is of the opinion that a product to which regulation 21 applies presents no risk to animal or public health, he or she may authorise that the product be used in accordance with regulation 26 of the Animal By-Products (Wales) Regulations 2006(20) notwithstanding paragraphs (2), (3) and (4) of regulation 21.

(2) The authorisation must be in writing, may be made subject to conditions, and may be amended, suspended or revoked by notice in writing at any time.

(3) The authorisation may specify which of the uses in regulation 26 of the Animal By-Products (Wales) Regulations 2006 is permitted.

Products containing unauthorised substances and excess residues

23.—(1) In this regulation—

(a) “maximum residue limit” (“terfyn gweddillion uchaf”) means a maximum residue limit listed in Annex I or Annex III to Council Regulation (EEC) No. 2377/90 (laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin)(21);

(b) “unauthorised substance” (“sylwedd anawdurdodedig”) has the same meaning as “unauthorised substance or product” in Council Directive 96/23/EC (on measures to monitor certain substances and residues thereof in live animals and animal products and repealing Directives 85/358/EEC and 86/469/EEC and Decisions 89/187/EEC and 91/664/EEC)(22); and

(c) “establishment of origin in a third country” (“sefydliad tarddiad mewn trydedd wlad”), means the establishment of origin in the third country of origin of the consignment, as set out in box 10 of the common veterinary entry document.

(2) This regulation applies where a veterinary check on a consignment from a particular establishment of origin in a third country reveals the presence of an unauthorised substance, or reveals that a maximum residue limit has been exceeded, but no Community measures have yet been adopted in response to this.

(3) In the circumstances described in paragraph (2), paragraphs (4), (5), (6) and (7) apply to those of the next ten consignments brought into the United Kingdom from that establishment which are brought into Wales.

(4) The official veterinary surgeon at the border inspection post at which any such consignment is brought in must, by notice in writing served on the person responsible for the consignment, take charge of it and check for unauthorised substances or their residues in the consignment by taking and analysing a representative sample of the products comprised in it.

(5) Upon service of a notice under paragraph (4), the person responsible for the consignment must lodge with the official veterinary surgeon a deposit or guarantee sufficient to assure payment of all charges payable in accordance with Part 9 for veterinary checks carried out on the consignment, including the taking of samples, and any laboratory test or analysis carried out on any sample taken.

(6) If any veterinary check carried out on the consignment reveals the presence of unauthorised substances or their residues or reveals that a maximum residue limit has been exceeded, the official veterinary surgeon must—

(a) redispatch the consignment, or such part of it as the official veterinary surgeon considers affected by the presence of unauthorised substances or their residues or by excess residues, accompanied by the required documents, to its third country of origin; and

(b) endorse on the required documents relating to the consignment a clear indication of the reasons for redispatching it.

(7) The cost of redispatching and transporting the consignment or part consignment to its third country of origin must be paid by the consignor whose name appears on the notice of the consignment’s introduction given under regulation 17.

Consignments and products illegally brought in

24.—(1) This regulation applies—

(a) where a consignment or product is brought into Wales from a third country but is not presented at a border inspection post in accordance with regulation 18;

(b) where a consignment or product originating in a third country has been brought into Wales from elsewhere in the relevant territories, but has not been presented at a border inspection post there;

(c) where the border inspection post of destination of a consignment of Article 9 products is in Wales but the consignment is not presented there in accordance with regulation 18; or

(d) where a consignment introduced into Wales is presented to the official veterinary surgeon at a border inspection post not designated and approved for veterinary checks on the products comprised within that consignment.

(2) In the circumstances described in paragraphs (1)(a), (b) and (c), an authorised officer must, by notice in writing served on the person appearing to have charge of the consignment or product, take charge of that consignment or product and either redispatch it in accordance with paragraph (5) or dispose of it in accordance with paragraph (4).

(3) In the circumstances described in paragraph (1)(d), the official veterinary surgeon must, by notice in writing served on the person responsible for the consignment, take charge of that consignment and either redispatch it in accordance with paragraph (5) or dispose of it in accordance with paragraph (4).

(4) Where the authorised officer or the official veterinary surgeon decides to dispose of the product or consignment, he or she must dispose of it as if it were Category 1 material under Regulation (EC) No. 1774/2002 in the facilities provided for that purpose nearest to the place at which the authorised officer or official veterinary surgeon takes charge of it.

(5) Where the authorised officer or the official veterinary surgeon decides to redispatch the product or consignment, he or she must do so—

(a) within a period of sixty days commencing with the day following the service of the notice;

(b) to a third country destination agreed with—

(i) the owner of the product or consignment, in the circumstances described in paragraphs (1)(a), (b) or (c); or

(ii) the person responsible for the consignment, in the circumstances described in paragraph (1)(d); and

(c) by the mode of transport by which the product or consignment was first brought into the relevant territories.

Products dangerous to animal or public health

25.  If an official veterinary surgeon or an authorised officer considers that a consignment or product from a third country presents a risk to animal or public health he or she must, by notice in writing served on the person appearing to have charge of it, take charge of it and dispose of it in accordance with regulation 24(4).

Serious or repeated infringements

26.—(1) Where the National Assembly or the Agency reasonably concludes, on the basis of the results of veterinary checks, that products from a particular third country, part of a third country or establishment in a third country are implicated in serious or repeated infringements of any requirement laid down in a Community instrument relating to animal or public health, this regulation applies to those of the next ten consignments brought into the United Kingdom from that third country, part of a third country or establishment, as the case may be, that are brought into Wales.

(2) The official veterinary surgeon at the border inspection post at which any such consignment is brought in must, by written notice served on the person responsible for the consignment, take charge of it and carry out a physical check upon it, including the taking of samples and laboratory tests and analyses.

(3) Upon service of a notice under paragraph (2) the person responsible for the consignment must lodge with the official veterinary surgeon a deposit or guarantee sufficient to assure payment of all charges payable in accordance with Part 9 for veterinary checks carried out on the consignment, including the taking of samples, and any laboratory test or analysis carried out on any sample taken.

(4) If any veterinary check carried out on the consignment reveals an infringement of any requirement laid down in a Community instrument relating to animal or public health, the official veterinary surgeon must either redispatch or dispose of the consignment in accordance with regulation 21(3).

Invalidation of veterinary documents

27.  Where an official veterinary surgeon or an authorised officer serves a notice requiring redispatch of a product under regulation 21(3)(a), or takes charge of a consignment under regulation 24(2), any person who has possession or control of the required documents relating to that product or consignment must immediately submit them to the official veterinary surgeon or authorised officer, as the case may be, for invalidation.

Costs in respect of products redispatched or disposed of

28.—(1) The persons specified in paragraph (2) must pay on demand the costs of storing, transporting, redispatching and disposing of any product, consignment or part consignment redispatched or disposed of—

(a) under regulation 21, 24, 25 or 26; or

(b) under the Customs and Excise Management Act 1979(23) in the enforcement of regulation 16.

(2) The persons referred to in paragraph (1) are—

(a) the person responsible for the product, consignment or part consignment in question;

(b) where a notice has been served on the person appearing to have charge of the product, consignment or part consignment, the owner of the product, consignment or part consignment; or

(c) the person on whom a notification of seizure has been served under the Customs and Excise Management Act 1979.

(3) Any cost referred to in paragraph (1) which is paid by an official veterinary surgeon, an authorised officer, the National Assembly, a local authority, the Agency or the Commissioners must be reimbursed on demand by, as the case may be, the person responsible for, or the owner of, the product, consignment or part consignment.

PART 4 The Disposal and Burial of Unused On-Board Catering Supplies and Other Material

Disposal of unused catering supplies

29.—(1) Part 3 does not apply in relation to products that are brought into Wales from means of transport operating internationally and that had been intended for consumption by the crew or passengers on that means of transport.

(2) Any person who has in his or her possession or under his or her control a product referred to in paragraph (1) must comply with Article 4(2) and (3) of Regulation (EC) No. 1774/2002.

(3) Where items such as packaging materials, or disposable cutlery or plates—

(a) have been in contact with a product referred to in paragraph (1); and

(b) are unloaded from the means of transport for disposal,

the person referred to in paragraph (2) must ensure that those items are dealt with in the same way as the products themselves.

Approval of landfills

30.—(1) Any person disposing of material in accordance with regulation 29 by burial in a landfill may only do so in a landfill approved under this regulation.

(2) The National Assembly may only approve a landfill for the purposes of disposal of material under regulation 29 if it is satisfied that—

(a) the material will be buried without undue delay so as to prevent access to it by wild birds;

(b) the operator has taken adequate steps to prevent access to the unrestored and current working area of the landfill by ungulates; and

(c) the operator will comply with any conditions of the approval.

(3) The approval must be in writing, may be made subject to conditions, and may be amended or suspended by notice in writing in accordance with regulation 32.

(4) If the National Assembly refuses to grant an approval, or grants an approval subject to a condition, it must by notice in writing served on the applicant-—

(a) give the reasons; and

(b) explain the right of the applicant to make written representations to the National Assembly and to appear before and be heard by an independent person appointed by the National Assembly in accordance with regulation 33.

Operators of landfills

31.—(1) The operator of a landfill approved in accordance with regulation 30 must-—

(a) maintain and operate the premises in accordance with the requirements in regulation 30(2)(a) and (b) and any conditions of the approval;

(b) ensure that any person employed by him or her, and any person permitted to enter the premises complies with those requirements and conditions;

(c) comply with the record-keeping requirements contained in Article 9 of Regulation (EC) No. 1774/2002; and

(d) keep equivalent records for material referred to in regulation 29(3).

(2) The records required to be kept under this regulation may be in written or electronic form and must be kept for at least two years.

Amendment, suspension and revocation of approvals

32.—(1) Where the National Assembly is satisfied that any condition of the approval is no longer fulfilled, or that the requirements in regulation 30(2)(a) and (b) are not being complied with, or that it is necessary to do so for public or animal health reasons, it may, by notice in writing served on the operator, suspend the approval.

(2) Where the National Assembly is satisfied that any condition of the approval should be amended for public or animal health reasons, it may, by notice in writing served on the operator, amend the approval.

(3) A suspension under paragraph (1) or an amendment under paragraph (2)-—

(a) has immediate effect if the National Assembly is satisfied that it is necessary for it to do so for the protection of public or animal health; and

(b) otherwise does not have effect for at least twenty-one days following service of the notice.

(4) The notice in paragraph 32(1) or (2) must-—

(a) give the reasons for the suspension or amendment; and

(b) explain the right of the operator of the premises to make written representations to the National Assembly and to be heard by an independent person appointed by the National Assembly in accordance with regulation 33.

(5) Where there is an appeal under regulation 33, an amendment or suspension does not have effect until the final determination by the National Assembly in accordance with that regulation unless the National Assembly considers it necessary for the protection of public or animal health for the amendment or suspension to take effect sooner.

(6) Where the National Assembly has suspended an approval, and-—

(a) no appeal is brought in accordance with regulation 33; or

(b) the National Assembly upholds the suspension following such an appeal,

it may by notice in writing revoke the approval provided that it is satisfied, taking into account all the circumstances of the case, that the premises will not be operated in accordance with the requirements of regulation 30(2)(a) or (b) or the conditions, if any, of the approval.

Appeals

33.—(1) A person on whom a notice is served under paragraph (4) of regulation 30 or paragraph (1) or (2) of regulation 32 may within twenty-one days beginning with the day on which the notice is served-—

(a) provide written representations to the National Assembly; and

(b) give notice in writing that he or she wishes to appear before and be heard by an independent person appointed by the National Assembly.

(2) Where an appellant gives notice of his or her wish to appear before and be heard by an independent person appointed for the purpose-—

(a) the National Assembly must appoint an independent person to hear representations and specify a time limit within which representations to that independent person must be made;

(b) the person so appointed must not, except with the consent of the appellant, be an officer or servant of the National Assembly;

(c) if the appellant so requests, the hearing must be in public;

(d) the independent person must report to the National Assembly; and

(e) if the appellant so requests, the National Assembly must provide him or her with a copy of the independent person’s report.

(3) The National Assembly must give to the appellant written notification of its final determination and the reasons for it.

PART 5 Products Intended for Import

Retention of documents at border inspection posts

34.  Where a documentary check has been carried out at a border inspection post on a product intended (whether directly or ultimately) for import, the person who presented the required documents relating to that product under regulation 18 must surrender the same to the official veterinary surgeon at that border inspection post.

Evidence of certification of, and payment for, veterinary checks

35.  Where Part 2 of the common veterinary entry document has been issued certifying that a consignment is fit for import, the person responsible for the consignment must ensure that the Commissioners have been supplied with evidence satisfactory to them that—

(a) Part 2 of that document has been issued; and

(b) payment of all charges payable in accordance with Part 9 of these Regulations for veterinary checks carried out on the consignment, including sampling, and for any test or analysis carried out on any samples taken—

(i) has been made; or

(ii) has been assured by a deposit or guarantee satisfactory to the person to whom, under regulation 54(2), the charges are payable.

Products not intended for the United Kingdom

36.—(1) Where—

(a) notice of bringing in a product has been given under regulation 17; and

(b) that notice specifies a member State other than the United Kingdom as the country of destination; and

(c) the circumstances mentioned in paragraph (2) apply,

no person may, without reasonable excuse, prevent or delay the transport of that product to that member State.

(2) The circumstances referred to in paragraph (1)(c) are that Part 2 of the common veterinary entry document has been issued in respect of that product, authorising its import—

(a) into that member State or a particular area of it in accordance with specific requirements; or

(b) for specific purposes in accordance with conditions,

and those requirements or conditions are laid down for products imported into that member State or particular area, or for products imported for those specific purposes, in any Directive, Decision or Regulation listed in Schedule 1.

Products transported under supervision

37.—(1) This regulation applies to products intended for import which are required by any Directive, Decision or Regulation listed in Schedule 1 to be transported under veterinary supervision from the border inspection post at which they are first brought into the relevant territories to their destination establishment.

(2) No person may remove a product to which this regulation applies from a border inspection post unless it is contained in a leak-proof container or a means of transport which has been sealed by an officer of Revenue and Customs or by the official veterinary surgeon at that border inspection post.

(3) The person responsible for a product to which this regulation applies and any carrier who has charge of it for the time being must ensure that the product is transported without delay to its destination establishment, and that the common veterinary entry document accompanies it until it reaches its destination establishment.

(4) Where Part 2 of the common veterinary entry document has authorised the import of a product to which this regulation applies for specific purposes as described in regulation 36(2)(b), the person responsible for the product and any carrier who has charge of it for the time being must ensure that it remains under the supervision of the Commissioners in accordance with the T5 procedure provided for in Articles 471 to 495 of Commission Regulation (EEC) No. 2454/93 (laying down provisions for the implementation of Council Regulation (EEC) No. 2913/92 establishing the Community Customs Code)(24) until it reaches its destination establishment.

(5) The operator of a destination establishment must give immediate written notification to the veterinary officer who is responsible on behalf of the National Assembly or the Agency for the destination establishment of the arrival there of any product to which this regulation applies.

(6) The operator of a destination establishment must ensure that a product to which this regulation applies undergoes at the destination establishment the treatment prescribed for it by the relevant Directive, Decision or Regulation listed in Schedule 1.

Transhipment of products intended for import

38.—(1) This regulation applies to transhipped products where the border inspection post of introduction is in Wales.

(2) As soon as a product to which this regulation applies arrives at the border inspection post of introduction, the person responsible for the product must notify the official veterinary surgeon there in writing, or in computerised or other electronic form, of the exact location of the product, of the estimated time of its transhipment or unloading, and of its border inspection post of destination.

(3) Where, according to the notification given under paragraph (2), a product to which this regulation applies is to be transhipped—

(a) from one aircraft to another, either directly or after being unloaded in a customs controlled area at the border inspection post of introduction for less than twelve hours; or

(b) from one sea-going vessel to another, either directly or after being unloaded in a customs controlled area at the border inspection post of introduction for less than seven days,

the conditions set out in paragraph (4) apply.

(4) The conditions referred to in paragraph (3) are that—

(a) where a person is required by regulation 18 to present the product and its required documents, to the official veterinary surgeon at the border inspection post of introduction, or to ensure that they are so presented; and

(b) the official veterinary surgeon considers that the product presents a risk to animal or public health,

the person mentioned in sub-paragraph (a) must permit the official veterinary surgeon, or an assistant appointed under regulation 6(1)(b) or 6(2)(c), to carry out a documentary check on the required documents.

(5) Paragraph (6) applies where it is proposed—

(a) to unload a product to which this regulation applies from an aircraft; and

(b) to reload that product onto an aircraft within a period of not less than twelve hours and no greater than 48 hours from the time it was unloaded.

(6) The person responsible for the product must ensure that—

(a) it is stored under the supervision of the official veterinary surgeon at the border inspection post of introduction in a customs controlled area there; and

(b) it is then reloaded onto an aircraft for onward transport to its border inspection post of destination.

(7) Paragraph (8) applies where it is proposed—

(a) to unload a product to which this regulation applies from a sea-going vessel; and

(b) to reload that product onto a sea-going vessel within a period of not less than seven days and no greater than twenty days from the time it was unloaded.

(8) The person responsible for the product must ensure that—

(a) it is stored under the supervision of the official veterinary surgeon at the border inspection post of introduction in a customs controlled area there; and

(b) it is then reloaded onto a sea-going vessel for onward transport to its border inspection post of destination.

(9) Any person required by regulation 18 to present a product to which paragraphs (5) and (6) or paragraphs (7) and (8) apply and its required documents to the official veterinary surgeon at a border inspection post of introduction must permit the official veterinary surgeon there, or an assistant appointed under regulation 6(1)(b) or 6(2)(c), to carry out a documentary check on the required documents and, if the official veterinary surgeon considers that the product presents a risk to animal health or public health, an identity check of the product against the required documents and a physical check of the product.

(10) Where it is proposed—

(a) to unload a product to which this regulation applies from an aircraft and to store that product for more than 48 hours after unloading; or

(b) to unload a product to which this regulation applies from a sea-going vessel and to store that product for more than twenty days after unloading,

any person required by regulation 18 to present the product and its required documents to the official veterinary surgeon at the border inspection post of introduction, must permit the official veterinary surgeon there, or an assistant appointed under regulation 6(1)(b) or 6(2)(c), to carry out in all cases, an identity check of the product against the required documents and a physical check of the product.

PART 6 Transit Products

Border inspection posts of entry and exit

39.  In this Part—

“border inspection post of entry” (“safle arolygu ar y ffin ar gyfer dod i mewn”) means the border inspection post at which a transit product enters the customs territory of the Community; and

“border inspection post of exit” (“safle arolygu ar y ffin ar gyfer ymadael”) means the border inspection post through which it is intended a transit product will leave the customs territory of the Community, as specified in the common veterinary entry document relating to that product.

Prior authorisation of transit

40.  No person may bring a transit product into Wales from a third country unless the official veterinary surgeon at the border inspection post of entry has previously authorised the transit of that product in writing.

Physical check of transit products

41.  Any person required by regulation 18 to present a transit product, or ensure that it is presented, to the official veterinary surgeon at the border inspection post of entry need only permit the official veterinary surgeon, or an assistant appointed under regulation 6(1)(b) or 6(2)(c), to carry out a physical check on the transit product if the official veterinary surgeon considers that it may present a risk to animal or public health or reasonably suspects some other irregularity, as defined in regulation 21(10), in relation to the transit product.

Movement of transit products

42.—(1) No person may remove, or cause to be removed, a transit product from the border inspection post of entry unless the person responsible for the product has given a written undertaking to the official veterinary surgeon there to observe and perform the requirements of regulation 43.

(2) Where, at any time after removal from a border inspection post of entry, a transit product is transported through Wales by road, rail, waterway or air—

(a) the person responsible for the transit product and any carrier who has charge of it for the time being must ensure that it is conveyed in a vehicle or container sealed by the Commissioners or by the veterinary authorities responsible for the border inspection post of entry, accompanied by its required documents, any translations required under regulation 18(4) and its common veterinary entry document, to the border inspection post of exit under the supervision of the Commissioners in accordance with the external transit procedure referred to in Articles 91 to 97 of the Customs Code;

(b) no person may—

(i) break the seals on the vehicle or container in which the transit product is conveyed;

(ii) unload the transit product;

(iii) split the consignment or part consignment which includes the transit product; or

(iv) subject the transit product to any form of handling; and

(c) the person responsible for the transit product and any carrier who has charge of it for the time being must ensure that it leaves the customs territory of the Community at the border inspection post of exit not more than 30 days after removal from the border inspection post of entry (excluding the day of removal).

(3) No person may bring a transit product into a free zone, a free warehouse or a customs warehouse in Wales.

Disposal of returned transit products

43.—(1) If a transit product is returned to Wales after leaving the customs territory of the Community, the person responsible for the transit product must either—

(a) redispatch the transit product from the border inspection post to which it is returned to a third country by the mode of transport by which it was returned within sixty days of its return (excluding the day of return); or

(b) if the circumstances described in paragraph (2) apply, dispose of the product as if it were Category 1 material under Regulation (EC) No. 1774/2002 in the facilities provided for that purpose nearest to the border inspection post to which the product is returned.

(2) The transit product must be disposed of in accordance with paragraph (1)(b) where—

(a) redispatch of the product is precluded on animal or public health grounds by the results of a physical check, or by any animal or public health requirement laid down in a Community instrument in force on the date on which these Regulations are made, or is otherwise impossible;

(b) the sixty day period referred to in paragraph (1)(a) has expired; or

(c) the person responsible for the transit product agrees immediately to its disposal.

(3) Any person who has possession or control of the required documents or the common veterinary entry document relating to a transit product to which paragraph (1) applies must submit them for invalidation to the official veterinary surgeon at the border inspection post to which the product is returned.

(4) The person responsible for a transit product to which paragraph (1) applies must store it until redispatch or destruction under the supervision of the official veterinary surgeon at the border inspection post to which the product is returned at such place and in such conditions as the official veterinary surgeon may direct.

(5) The person responsible for a transit product to which paragraph (1) applies must pay the costs of storing, transporting, redispatching and disposing of it.

PART 7 Products Intended for Warehouses, Ships' Stores or Cross-Border Means of Sea Transport

Application of Part 7

44.  This Part applies to products whose destination establishment is—

(a) a warehouse in a free zone, a free warehouse or a customs warehouse, located in the customs territory of the Community;

(b) a ships' store complying with Article 13 of Directive 97/78/EC located outside the United Kingdom; or

(c) a cross-border means of sea transport.

Additional information to be given in advance

45.—(1) No person may bring a product to which this Part applies into Wales, or present such a product to a border inspection post of destination in Wales, unless the official veterinary surgeon to whom notice of the product’s introduction or presentation is given under regulation 17 has been informed—

(a) whether the product is intended ultimately for import;

(b) if not, whether it is a transit product, or a product whose destination establishment is a cross-border means of sea transport; and

(c) in any event whether the product complies with the import conditions.

(2) The information in paragraph (1) must be given in writing and may be included in the notice of the product’s introduction or presentation given under regulation 17.

Physical check of non-conforming products

46.  Where the required documents indicate that a product to which this Part applies is a non-conforming product, any person required by regulation 18 to present it, or ensure that it is presented, to the official veterinary surgeon at a border inspection post need only permit the official veterinary surgeon, or an assistant appointed under regulation 6(1)(b) or 6(2)(c), to carry out a physical check on the product if the official veterinary surgeon considers that it may present a risk to animal health or public health.

Exclusion of non-conforming products from warehouses

47.  No person may bring a non-conforming product into a warehouse in a free zone, a free warehouse or a customs warehouse in Wales.

Direct movement to cross border means of sea transport

48.  No person may move a product whose destination establishment is a cross-border means of sea transport from the border inspection post at which it was brought in other than directly and without delay to that cross-border means of sea transport.

Additional certificate to accompany products on board means of sea transport

49.—(1) The person responsible for a product or a consignment of products whose destination establishment is a cross-border means of sea transport, and any carrier who has charge of such a product or consignment for the time being, must ensure that the certificate referred to in Article 13(2)(a) of Directive 97/78/EC, which must be based on the model in the Annex to Commission Decision 2000/571/EC(25), accompanies the product or consignment from the border inspection post from which it is dispatched until it is delivered on board the means of sea transport.

(2) On delivery of the product or consignment on board the means of sea transport, the master of that means of sea transport, or an official representative of the master, must confirm delivery of the product or consignment by countersigning the certificate referred to in paragraph (1) and returning it as soon as reasonably practicable to the official veterinary surgeon at the border inspection post from which the product or consignment was dispatched (as indicated in the certificate).

(3) The requirements of this regulation apply in addition to the requirements of regulation 20 (relating to the common veterinary entry document).

PART 8 Products Returned from Third Countries

Meaning of “export certificate”

50.  In this Part, “export certificate”, in relation to a returned product, means a certificate—

(a) issued by the authorities in the original country of export; and

(b) declaring that the returned product complies with the relevant animal or public health standards of the country of receipt to which the product was originally exported.

Additional documentation for returned products

51.  Any person who presents under regulation 18 a returned product and its required documents to an official veterinary surgeon must present with the required documents—

(a) the export certificate relating to the returned product or a copy authenticated as true by the authority which issued it;

(b) a statement of the reasons why the returned product was refused by the third country;

(c) a declaration by the person responsible for the returned product that, since the returned product was originally exported from the customs territory of the Community, the import conditions relating to storage and transport have been complied with in relation to the returned product; and either

(d) in the case of a returned product not originally exported in a sealed container, a declaration by the person responsible for the returned product that it has not undergone any handling other than, in the case only of packaged products, loading and unloading of unopened packages; or

(e) in the case of a returned product originally exported in a sealed container, a declaration by the carrier who brought it into Wales that it has not been unloaded from the container in which it was exported, or otherwise handled.

Physical check of returned products

52.  Any person required by regulation 18 to present a returned product, or ensure that it is presented, to the official veterinary surgeon at a border inspection post need only permit the official veterinary surgeon, or an assistant appointed under regulation 6(1)(b) or 6(2)(c), to carry out a physical check on the returned product if the official veterinary surgeon has reasonable grounds for believing—

(a) that these Regulations have not been, or are not being, complied with in relation to the returned product;

(b) that the returned product does not comply with the import conditions; or

(c) that the identity or destination of the returned product does not correspond with the information given in any relevant document.

Movement of returned products

53.—(1) No person may remove, or cause to be removed, a returned product from a border inspection post—

(a) without the written authorisation of the official veterinary surgeon there; and

(b) unless it is contained in a leak-proof container or a means of transport which has been sealed by an officer of Revenue and Customs or by the official veterinary surgeon at that border inspection post.

(2) The person responsible for a returned product removed in accordance with paragraph (1), and any carrier who has charge of it for the time being, must ensure that—

(a) it is conveyed directly to its Community establishment of origin in the sealed leak-proof container or means of transport referred to in paragraph (1)(b); and

(b) its common veterinary entry document accompanies it until the returned product reaches its Community establishment of origin.

(3) No person may—

(a) break the seals on the container or means of transport in which the returned product is conveyed;

(b) unload the returned product;

(c) split the consignment or part consignment which includes the returned product; or

(d) subject the returned product to any form of handling,

until the product reaches its Community establishment of origin.

(4) The operator of the Community establishment of origin must give immediate written notification of the arrival there of the returned product to the veterinary officer who is responsible on behalf of the National Assembly or the Agency for that establishment.

PART 9 Charges for Veterinary Checks

Payment of charges

54.—(1) A reasonable charge calculated in accordance with regulations 55 and 56 and Schedule 3 must be made for veterinary checks carried out on a consignment at a border inspection post.

(2) The charge must be made by and payable to the National Assembly, a local authority or the Agency, whichever is responsible, under regulation 5, for enforcing these Regulations at the border inspection post where the veterinary checks are carried out.

Calculation of charges

55.  The charge for veterinary checks must cover the costs listed in Part I of Schedule 3 and must be calculated in accordance with Part II, III, IV or V, as the case may be, of Schedule 3.

Conversion of charges to sterling

56.  Charges expressed in euro in Schedule 3 must be converted to pounds sterling at the rate of conversion published in the “C” Series of the Official Journal of the European Communities in September of the calendar year preceding that in which the relevant veterinary check was carried out.

Liability for charges

57.  The person responsible for a consignment must pay on demand the charge made for the veterinary checks carried out on the consignment.

Information relating to charges

58.—(1) The National Assembly, a local authority or the Agency must, if so requested in writing, supply to any person who presents products under regulation 18, or to any organisation representing such persons, details of the calculations which he or she or it uses to determine charges for veterinary checks and must take into account any representations made by such a person or organisation in determining such charges.

(2) If requested in writing so to do by the National Assembly or the Agency, a local authority must provide the National Assembly or the Agency, as the case may be, with such information as it may require relating to the calculation of charges for veterinary checks, and with copies of any written representations made by persons or organisations referred to in paragraph (1).

Appeals against charges paid to local authorities

59.—(1) Any person who has paid a charge for veterinary checks to a local authority, and any organisation representing such persons, may, within twenty-one days of the charge being made, appeal in writing on the ground that the amount of the charge is unreasonable—

(a) to the National Assembly, where the charge is for veterinary checks carried out otherwise than in relation to any function of the Agency; and

(b) to the Agency, where the charge is for veterinary checks carried out in relation to any function of the Agency.

(2) Where there is an appeal under paragraph (1), the National Assembly or the Agency, as the case may be, must—

(a) consult with the local authority; and

(b) if satisfied that the amount of the charge is unreasonable, so inform the local authority.

(3) When informed under paragraph (2)(b), the local authority must—

(a) recalculate the amount of the charge in accordance with any directions given by the National Assembly or the Agency, as the case may be; and

(b) repay to the person who has paid the charge the difference between the original charge and the recalculated charge.

Appeals against charges paid to the National Assembly or the Agency

60.—(1) Any person who has paid a charge for veterinary checks to the National Assembly or the Agency, and any organisation representing such persons, may, within twenty-one days of the charge being made, give notice in writing of his or her wish to appeal to an independent person appointed by the National Assembly, or, where the charge was paid to the Agency, to an independent person appointed by the Agency, on the ground that the amount of the charge is unreasonable.

(2) Where the charge was paid to the Agency, the functions of the National Assembly in paragraphs (3) to (4) must be performed by the Agency.

(3) Where an appellant gives notice of his or her wish to appear before and be heard by an independent person appointed for the purpose-—

(a) the National Assembly must appoint an independent person to hear representations and specify a time limit within which representations to that independent person must be made;

(b) the person so appointed must not, except with the consent of the appellant, be an officer or servant of the National Assembly;

(c) if the appellant so requests, the hearing must be in public;

(d) the independent person must report to the National Assembly; and

(e) if the appellant so requests, the National Assembly must provide him or her with a copy of the independent person’s report.

(4) If the independent person is satisfied that the amount of the charge is unreasonable, the National Assembly must recalculate the charge in accordance with any directions given by the independent person and repay to the person who has paid the charge the difference between the original charge and the recalculated charge.

PART 10 Emergency Declarations

Disease outbreaks in third countries

61.—(1) Where the National Assembly or the Agency learns of, or has reasonable grounds to suspect, the presence in any third country of—

(a) a disease referred to in Council Directive 82/894/EEC (on the notification of animal diseases within the Community)(26); or

(b) a zoonosis or other disease, phenomenon or circumstance liable to present a serious threat to animal or public health,

or if any other serious animal health or public health reason so warrants, it may by declaration suspend, or impose conditions on, the bringing into Wales of any product from the whole or any part of that third country.

(2) Such a declaration must—

(a) be in writing;

(b) be published in such a manner as the National Assembly or the Agency, as the case may be, thinks fit; and

(c) must specify the products and the third country or part of the third country concerned.

(3) A declaration which imposes conditions on bringing any product from a third country or part of a third country into Wales must specify those conditions.

(4) Where a declaration is in force suspending the introduction of any product, no person may bring that product into Wales if it originates in the third country or part of the third country specified in the declaration.

(5) Where a declaration is in force imposing conditions on the introduction of any product, no person may bring that product into Wales if it originates in the third country or part of the third country specified in the declaration unless the product complies with the conditions specified in the declaration.

(6) A declaration may be modified, suspended or revoked by a further written declaration published, so far as is practicable, in the same manner and to the same extent as the original declaration.

PART 11 Offences and Penalties

Obstruction

62.  No person may—

(a) intentionally obstruct any person in the exercise of a power conferred by regulation 8 or 9 or in the performance of any other regulatory function;

(b) without reasonable cause fail to comply with a requirement made of him or her under regulation 8 or 9, or fail to give to any person exercising a power conferred by those regulations or performing any other regulatory function such assistance or information as that person may reasonably require of him or her for the purpose of exercising the power or performing the function; or

(c) furnish to any person exercising a power conferred by regulation 8 or 9 or performing any other regulatory function any information which he or she knows to be false or misleading.

Defences

63.—(1) In any proceedings for an offence of contravening a provision of the regulations listed in Schedule 4, it is a defence for the person charged to prove that he or she took all reasonable precautions and exercised all due diligence to avoid the commission of the offence by himself or herself or by a person under his or her control.

(2) If in any case the defence provided by paragraph (1) involves the allegation that the commission of the offence was due to an act or default of another person, or to reliance on information supplied by another person, the person charged is not, without leave of the Court, entitled to rely on that defence, unless—

(a) at least seven clear days before the hearing; and

(b) where he or she has previously appeared, or been brought, before a court in connection with the alleged offence, within one month of his or her first such appearance,

he or she has served on the prosecutor a notice in writing giving such information identifying or assisting in the identification of that other person as was then in his or her possession.

(3) In any proceedings for an offence of contravening regulation 5(9), it is a defence for the person charged to prove that he or she reasonably believed—

(a) that the disclosure was lawful; or

(b) that the information had already lawfully been made available to the public.

Contraventions

64.  Any person who—

(a) contravenes a provision of these Regulations, other than—

(i) the provisions contained in regulations 8(3) and 19(3) referring to payment of costs; and

(ii) the provisions contained in regulations 23(7), 28, 43(5), 45(2) and 57; or

(b) fails to comply with a notice served upon him or her under these Regulations,

is guilty of an offence.

Penalties

65.—(1) A person guilty of the offence of contravening regulation 62(a) or (b) is liable on summary conviction to a fine not exceeding level 5 on the standard scale or to imprisonment for a term not exceeding three months, or to both.

(2) A person guilty of any other offence under these Regulations is liable—

(a) on summary conviction, to a fine not exceeding the statutory maximum, to imprisonment for a term not exceeding three months or to both;

(b) on conviction on indictment, to imprisonment for a term not exceeding two years, to a fine or to both.

Offences by bodies corporate

66.—(1) If an offence under these Regulations committed by a body corporate is shown—

(a) to have been committed with the consent or connivance of an officer, or

(b) to be attributable to any neglect on his or her part,

the officer as well as the body corporate is guilty of the offence and liable to be proceeded against and punished accordingly.

(2) If the affairs of a body corporate are managed by its members, paragraph (1) applies in relation to the acts and defaults of a member in connection with his or her functions of management as if he or she were a director of the body.

(3) “Officer”, in relation to a body corporate, means a director, member of the committee of management, chief executive, manager, secretary or other similar officer of the body, or a person purporting to act in any such capacity.

Offences by Scottish partnerships

67.  Where an offence under these Regulations which has been committed by a Scottish partnership is proved to have been committed with the consent or connivance of, or to be attributable to any neglect on the part of, a partner, he or she, as well as the partnership is deemed to be guilty of that offence and liable to be proceeded against and punished accordingly.

PART 12 Notices and Decisions

Service of notices

68.—(1) Any notice served under these Regulations by the National Assembly, the Agency, an official veterinary surgeon, an official fish inspector or an authorised officer may be served on a person by—

(a) delivering it to that person;

(b) leaving it at his or her proper address; or

(c) posting it to his or her proper address.

(2) Any such notice which is to be served on a body corporate or an unincorporated association other than a partnership must be duly served on the secretary or clerk or other similar officer of that body.

(3) Any such notice which is to be served on a partnership (including a Scottish partnership) must be duly served on a partner or a person having the control or management of the partnership business.

(4) Subject to paragraphs (5) and (6), for the purposes of this regulation, the proper address of any person on whom a notice is to be served is his or her last known address, except that the proper address is—

(a) in the case of a body corporate or their secretary or clerk, the address of the registered office or principal office of the body corporate;

(b) in the case of an unincorporated association (other than a partnership) or their secretary or clerk, the address of the principal office of the association; and

(c) in the case of a partnership (including a Scottish partnership) or a person having the control or management of the partnership business, the address of the principal office of the partnership.

(5) Where the person to be served is a company registered, or a partnership carrying on business, outside the United Kingdom, and the company or partnership has an office within the United Kingdom, the principal office of that company or partnership for the purposes of paragraph (4) is its principal office within the United Kingdom.

(6) If the person to be served with any such notice has furnished the person by whom the notice is to be served with an address under any provision of these Regulations, that address must be treated as his or her proper address for the purposes of this regulation.

(7) For the purposes of this regulation, “posting” (“postio”), in relation to a notice, means sending it pre-paid by a postal service which seeks to deliver documents by post within the United Kingdom no later than the next working day in all or the majority of cases, and to deliver documents by post outside the United Kingdom within such period as is reasonable in all the circumstances.

Notification of decisions

69.  Where, under any provision of these Regulations, a decision is taken in relation to a product or consignment, the person taking the decision must notify the person responsible for the product or consignment in writing of the decision and the reasons for it, together with details of his or her right of appeal against the decision including the procedure and time limits applicable.

PART 13 Disapplications and Revocations

Disapplication of existing provisions

70.—(1) The Importation of Embryos, Ova and Semen Order 1980(27) does not apply to products to which these Regulations apply, except embryos, ova and semen of the ovine and caprine species.

(2) The Importation of Animal Products and Poultry Products Order 1980(28) does not apply to products to which these Regulations apply, except the products referred to in regulation 4(7) of these Regulations.

(3) The following do not apply to products to which these Regulations apply—

(a) the Importation of Bovine Semen Regulations 1984(29); and

(b) the Importation of Processed Animal Protein Order 1981(30).

Revocations

71.  The Products of Animal Origin (Third Country Imports) (Wales) Regulations 2005(31) are revoked.

Signed on behalf of the National Assembly for Wales under section 66(1) of the Government of Wales Act 1998(32)

D. Elis-Thomas

Ben Bradshaw

The Presiding Officer of the National Assembly

13 February 2007

Regulations 2, 4(7), 21, 36, and 37

SCHEDULE 1 Import Conditions

PART I PROVISIONS COMMON TO SEVERAL CATEGORIES OF PRODUCT

Maximum residue limits and contaminants

1.  Council Regulation (EEC) No. 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin (OJ No. L224, 18.8.90, p. 1) as last amended by Commission Regulation (EC) No. 1451/2006 (OJ No. L271, 30.9.2006, p.37).

2.  Council Directive 96/23/EC on measures to monitor certain substances and residues thereof in live animals and animal products and repealing Directives 85/358/EEC and 86/469/EEC and Decisions 89/187/EEC and 91/664/EEC (OJ No. L125, 23.5.96, p. 10) as last amended by Regulation (EC) No. 882/2004 of the European Parliament and of the Council (see Corrigendum OJ No. L191, 28.5.2004, p. 1).

3.  Commission Regulation (EC) No. 466/2001 setting maximum levels for certain contaminants in foodstuffs (OJ No. L77, 16.3.2001, p. 1) as last amended by Commission Regulation (EC) No. 199/2006, (OJ No. L32, 4.2.2006, p. 34).

4.  Commission Decision 2004/432/EC on the approval of residue monitoring plans submitted by third countries in accordance with Council Directive 96/23/EC (OJ No. L154, 30.4.2004, p. 44) as last amended by Commission Decision 2006/208/EC (OJ No. L75, 14.3.2006, p. 20).

5.  Commission Decision 2005/34/EC laying down harmonised standards for the testing for certain residues in products of animal origin imported from third countries (OJ No. L16, 20.1.2005, p. 61).

Transmissible spongiform encephalopathies

6.  Regulation (EC) No. 999/2001 of the European Parliament and of the Council laying down rules for the prevention, control, and eradication of certain transmissible spongiform encephalopathies (OJ No. L147, 31.5.2001, p. 1) as last amended by Commission Regulation (EC) (No.) 1041/2006 (OJ No. L187, 8.7.2006, p. 10).

Health certification for animal products from New Zealand

7.  Commission Decision 2003/56/EC on health certificates for the importation of live animals and animal products from New Zealand (OJ No. L22, 25.1.2003, p. 38) as last amended by Commission Decision 2004/784/EC (OJ No. L346, 23.11.2004, p. 11).

Animal health rules on imports of products of animal origin for human consumption

8.  Council Directive 2002/99/EC laying down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption (OJ No. L18, 23.1.2003, p. 11) as last amended by Council Regulation (EC) No. 882/2004 (OJ No. L191, 28.5.2004, p. 1).

9.  Regulation (EC) No. 178/2002 of the European Parliament and of the Council laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (OJ No. L31, 1.2.2002, p. 1).

10.  Council Regulation (EC) No. 183/2005 (laying down requirements for feed hygiene (OJ No. L35, 8.2.2005, p. 1).

11.  Council Regulation (EC) No. 396/2005 on maximum levels of pesticides in or on food and feed of plant and animal origin and amending Council Directive 91/414/EEC (OJ No. L70, 16.3.2005, p. 1) as amended by Regulation (EC) No 178/2006 (OJ No. L29, 2.2.2006, p. 3).

Public health rules on imports of products of animal origin for human consumption

12.  Regulation (EC) No. 853/2004 of the European Parliament and the Council laying down specific hygiene rules for food of animal origin (OJ No. L139, 30.4.2004, p. 55) as last amended by Regulation 2076/2005 (OJ No. L338, 22.12.2005, p. 83).

13.  Regulation (EC) No. 854/2004 of the European Parliament and the Council laying down specific hygiene rules for the organisation of official controls on products of animal origin intended for human consumption (OJ No. L139, 30.4.2004, p. 206) as last amended by Regulation (EC) 2076/2005 (OJ No. L338, 22.12.2005, p. 83).

14.  Regulation (EC) No. 882/2004 of the European Parliament and the Council on official controls performed to ensure the verification of compliance with feed and food law, animal health and animal welfare rules (OJ No. L191, 28.5.2004, p. 1).

15.  Commission Regulation (EC) No. 2073/2005 on microbiological criteria for foodstuffs (OJ No. L338, 22.12.2005, p. 1).

16.  Commission Regulation (EC) No. 2074/2005 laying down implementing measures for certain products under Regulation (EC) No. 853/2004 of the European Parliament and of the Council and for the organisation of official controls under Regulation (EC) No. 854/2005 of the European Parliament and of the Council and Regulation 882/2004 of the European Parliament and of the Council, derogating from Regulation 852/2004 of the European Parliament and of the Council and amending Regulations (EC) 853/2004 and (EC) 854/2004 (OJ No. L338, 22.12.2005, p. 27).

17.  Commission Regulation (EC) No. 2075/2005 laying down specific rules on official controls for Trichinella in meat (OJ No. L338, 22.12.2005, p. 60).

18.  Commission Regulation (EC) No. 2076/2005 laying down transitional arrangements for the implementation of Regulations (EC) No. 853/2004, (EC) No. 854/2004 and (EC) No. 882/2004 of the European Parliament and of the Council and amending Regulations (EC) No 853/2004 and (EC) No 854/2004 (OJ No. L338, 22.12.2005, p. 83).

PART II FRESH MEAT OF BOVINE, OVINE AND CAPRINE ANIMALS AND SWINE

Third countries from which fresh meat may be imported

1.  Council Decision 79/542/EEC drawing up a list of third countries or parts of third countries, and laying down animal and public health and veterinary certification conditions, for importation into the Community of certain live animals and their fresh meat (OJ No. L146, 14.6.79, p. 15) as last amended by Commission Decision 2006/463/EC (OJ No. L183, 5.7.2006, p. 20).

Third country establishments from which fresh meat may be imported

2.  Regulation (EC) No. 854/2004 (see paragraph 13 of Part I).

3.  Argentina— Commission Decision 81/91/EEC (OJ No. L58, 5.3.81, p. 39) as amended by Commission Decision 86/392/EEC (OJ No. L228, 14.8.86, p. 44).

4.  Australia— Commission Decision 83/384/EEC (OJ No. L222, 13.8.83 p. 36) as amended by Commission Decision 86/389/EEC (OJ No. L228, 14.8.86, p. 34).

5.  Botswana— Commission Decision 83/243/EEC (OJ No. L129, 19.5.83, p. 70).

6.  Brazil— Commission Decision 81/713/EEC (OJ No. L257, 10.9.81, p. 28) as last amended by Commission Decision 89/282/EEC (OJ No. L110, 21.4.89, p. 54).

7.  Bulgaria— Commission Decision 87/735/EEC (OJ No. L311, 8.11.82, p. 16).

8.  Canada— Commission Decision 87/258/EEC (OJ No. L121, 9.5.87, p. 50).

9.  Chile— Commission Decision 87/124/EEC (OJ No. L51, 20.2.87, p. 41).

10.  Croatia— Commission Decision 93/26/EEC (OJ No. L16, 25.1.93, p. 24).

11.  The Falkland Islands— Commission Decision 2002/987/EC (OJ No. L344, 19.12.2002, p. 39).

12.  Greenland— Commission Decision 85/539/EEC (OJ No. L334, 12.12.85, p. 25).

13.  Iceland— Commission Decision 84/24/EEC (OJ No. L20, 25.1.84, p. 21).

14.  Former Yugoslav Republic of Macedonia— Commission Decision 95/45/EC (OJ No. L51, 8.3.95, p. 13).

15.  Madagascar— Commission Decision 90/165/EEC (OJ No. L91, 6.4.90, p. 34).

16.  Mexico— Commission Decision 87/424/EEC (OJ No. L228, 15.8.87, p. 43).

17.  Morocco— Commission Decision 86/65/EEC (OJ No. L72, 15.3.86, p. 40).

18.  Namibia— Commission Decision 90/432/EEC (OJ No. L223, 18.8.90, p. 19).

19.  New Caledonia— Commission Decision 2004/628/EC (OJ No. L284, 3.9.2004, p. 4).

20.  New Zealand— Commission Decision 83/402/EEC (OJ No. L223, 24.8.83, p. 24) as amended by Commission Decision 86/432/EEC (OJ No. L253, 5.9.86, p. 28).

21.  Paraguay— Commission Decision 83/423/EEC (OJ No. L238, 27.8.83, p. 39).

22.  Romania— Commission Decision 83/218/EEC (OJ No. L121, 7.5.83, p. 23) as amended by Commission Decision 86/289/EEC (OJ No. L182, 5.7.86, p. 25).

23.  South Africa— Commission Decision 82/913/EEC (OJ No. L381, 31.12.82, p. 28) as amended by Commission Decision 90/433/EEC (OJ No. L223, 18.8.90, p. 21).

24.  Swaziland— Commission Decision 82/814/EEC (OJ No. L343, 4.12.82, p. 24).

25.  Switzerland— Commission Decision 82/734/EEC (OJ No. L311, 8.11.82, p. 13) as last amended by Commission Decision 92/2/EEC (OJ No. L1, 4.1.92, p. 22).

26.  United States of America— Commission Decision 87/257/EEC (OJ No. L121, 9.5.87, p. 46) as amended by Commission Decision 2000/138/EC (OJ No. L46, 18.2.2000, p. 36).

27.  Uruguay— Commission Decision 81/92/EEC (OJ No. L58, 5.3.81, p. 43) as amended by Commission Decision 86/485/EEC (OJ No. L282, 3.10.86, p. 31).

28.  Federal Republic of Yugoslavia— Commission Decision 98/8/EEC (OJ No. L2, 6.1.98, p. 12).

29.  Zimbabwe— Commission Decision 85/473/EEC (OJ No. L278, 18.10.85, p. 35).

Health certification requirements

30.  Council Decision 79/542/EEC (see paragraph 1 of this Part).

31.  Canada (pig meat)— Commission Decision 2005/290/EC on simplified certificates for the importation of bovine semen and fresh pig meat from Canada and amending Decision 2004/639/EC (OJ No. L93, 12.4.2005, p. 34).

PART III MEAT PRODUCTS

Third countries from which meat products may be imported

1.  Commission Decision 2005/432/EC laying down the animal and public health conditions and model certificates for imports of meat products for human consumption from third countries and repealing Decisions 97/41/EC, 97/221/EC and 97/222/EC (OJ No. L151, 14.6.2005, p. 3) as amended by Commission Decision 2006/330/EC (OJ No. L121, 6.5.2006, p. 43).

Third country establishments from which meat products may be imported

2.  Argentina— Commission Decision 86/414/EEC (OJ No. L237, 23.8.86, p. 36), as amended by Commission Decision 97/397/EC (OJ No. L165, 24.6.97, p. 13).

3.  Botswana— Commission Decision 94/465/EC (OJ No. L190, 26.7.94, p. 25).

4.  Brazil— Commission Decision 87/119/EC (OJ No. L49, 18.2.87, p. 37) as amended by Commission Decision 95/236/EC (OJ No. L156, 7.7.95, p. 85).

5.  Namibia— Commission Decision 95/427/EC (OJ. No. L254, 24.10.95, p. 28).

6.  Uruguay— Commission Decision 86/473/EEC (OJ No. L279, 30.9.86, p. 53) as amended by Commission Decision 96/466/EC (OJ No. L192, 2.8.96, p. 25).

7.  Zimbabwe— Commission Decision 94/40/EC (OJ No. L22, 27.1.94, p. 50).

8.  Miscellaneous third countries— Commission Decision 97/365/EC (OJ No. L154, 12.6.97, p. 41) as last amended by Commission Decision 2004/380/EC (OJ No. L144, 30.4.2004, p. 5).

9.  Miscellaneous third countries— Commission Decision 97/569/EC (OJ No. L234, 26.8.97, p. 16) as last amended by Commission Decision 2005/787/EC (OJ No. L296, 12.11.2005, p. 39).

Health Certification Requirements

10.  Commission Decision 2005/432/EC (see paragraph 1 of this Part).

PART IV MILK AND DAIRY PRODUCTS

General

1.  Commission Decision 2004/438/EC laying down animal and public health and veterinary certification conditions for introduction in the Community of heat-treated milk, milk-based products and raw milk intended for human consumption (OJ No. L154, 30.4.2004, p. 72) as amended by Commission Decision 2006/295/EC (OJ No. L108, 21.4.2006, p. 108).

Third countries from which milk and milk-based products may be imported

2.  Commission Decision 2004/438/EC (see paragraph 1 of this Part).

Third country establishments from which milk and milk-based products may be imported

3.  Commission Decision 97/252/EC (OJ No. L101, 18.4.97, p. 46) as last amended by Commission Decision 2004/807/EC (OJ No. L354, 30.11.2004, p. 32).

PART V FRESH POULTRYMEAT

General

1.  Commission Decision 93/342/EC laying down the criteria for classifying third countries with regard to avian influenza and Newcastle disease (OJ No. L137, 8.6.93 p. 24) as amended by Commission Decision 94/438/EC (OJ No. L181, 15.7.94, p. 35).

Third countries from which fresh poultrymeat may be imported

2.  Commission Decision 94/85/EC (OJ No. L44, 17.2.94, p. 31) as last amended by Commission Decision 2004/118/EC (OJ No. L36, 7.2.2004, p. 34).

Third country establishments from which fresh poultrymeat may be imported

3.  Commission Decision 97/4/EC (OJ No. L2, 4.1.97, p. 6) as last amended by the Act concerning the conditions of accession of the Czech Republic, the Republic of Estonia, the Republic of Cyprus, the Republic of Latvia, the Republic of Lithuania, the Republic of Hungary, the Republic of Malta, the Republic of Poland, the Republic of Slovenia and the Slovak Republic and the adjustments to the Treaties on which the European Union is founded (OJ No. L236, 23.9.2003, p. 33) (“the Act of Accession”).

Health certification requirements

4.  Commission Decision 94/984/EC (OJ No. L378, 31.12.94, p. 11) as last amended by Commission Decision 2004/436/EC (OJ No. L154, 30.4.2004, p. 59).

PART VI WILD GAME MEAT

General

1.  Commission Decision 2000/585/EC drawing up a list of third countries from which member States authorise imports of rabbit meat and certain wild and farmed game meat, and laying down the animal and public health and the veterinary certification conditions for such imports (OJ No. L251, 6.10.2000, p. 1) as last amended by Commission Decision 2004/413/EC (OJ No. L151, 30.4.2004, p. 54).

Third country establishments from which game meat may be imported

2.  Commission Decision 97/468/EC (OJ No. L199, 26.7.97, p. 62) as last amended by the Act of Accession (see paragraph 3 of Part V).

PART VII MINCED MEAT AND MEAT PREPARATIONS

Health certification requirements

1.  Commission Decision 2000/572/EC (OJ No. L240, 23.9.2000, p. 19) as last amended by Commission Decision 2004/437/EC (OJ No. L154, 30.4.2004, p. 65) (meat preparations).

2.  Council Decision 79/542/EEC (see paragraph 1 of Part II) (minced meat).

Third country establishments from which minced meat and meat preparations may be imported

3.  Commission Decision 99/710/EC (OJ No. L281, 4.11.99, p. 82) as last amended by Commission Decision 2005/156/EC (OJ No. L51, 24.2.2005, p. 26).

PART VIII MISCELLANEOUS PRODUCTS

General

1.  Council Directive 92/118/EEC laying down animal and public health requirements governing trade in and imports into the Community of products not subject to the said requirements laid down in specific Community rules referred to in Annex A (1) to Directive 89/662/EEC and, as regards pathogens, to Directive 90/425/EEC (OJ No. L62, 15.3.93, p. 49) as last amended by Council Directive 2004/41/EC (OJ No. L195, 2.6.2004, p. 12).

2.  Commission Decision 2000/609/EC laying down animal and public health conditions and veterinary certification for imports of farmed ratite meat and amending Decision 94/85/EC drawing up a list of third countries from which member States authorise imports of fresh poultrymeat (OJ No. L258, 12.10.2000, p. 49) as last amended by Commission Decision 2005/804/EC (OJ No. L303, 22.11.2005, p. 56).

3.  Commission Decision 2005/760/EC concerning certain protection measures in relation to highly pathogenic avian influenza in certain third countries for the import of captive birds (OJ No. L285, 28.10.2005, p. 60) (in so far as it relates to products derived from those birds) as last amended by Commission Decision 2006/522/EC (OJ No. L205, 27.7.2006, p. 28).

Third countries from which products covered by Council Directive 92/118/EEC may be imported

4.  Commission Decision 2003/812/EC (OJ No. L305, 22.11.2003, p. 17) as amended by Commission Decision 2004/19/EC (OJ No. L5, 9.1.2004, p. 84).

Third country establishments from which products covered by Council Directive 92/118/EEC may be imported

5.  Commission Decision 97/467/EC (OJ No. L199, 26.7.97, p. 57) as last amended by Commission Decision 2006/65/EC (OJ No. L32, 4.2.2006, p. 93) (rabbit meat and farmed game meat).

6.  Commission Decision 99/120/EC (OJ No. L36, 10.2.99, p. 21) (animal casings) as last amended by Commission Decision 2005/506/EC (OJ No. L184, 15.7.2005, p. 68).

7.  Commission Decision 2001/396/EC (OJ No. L139, 23.5.2001, p. 16) (ratite meat).

8.  Commission Decision 2001/556/EC (OJ No. L200, 25.7.2001, p. 23) (gelatine) as last amended by Commission Decision 2005/33/EC (OJ No. L16, 20.1.2005, p. 59).

Health certification requirements

9.  Commission Decision 97/38/EC (OJ No. L14, 17.1.97, p. 61) (egg products).

10.  Commission Decision 2000/585/EC (see paragraph 1 of Part VI) (rabbit meat, feathered game meat and certain land mammals).

11.  Commission Decision 2000/609/EC (farmed ratite meat) (see paragraph 2 of this Part).

12.  Commission Decision 2003/779/EC (OJ No. L285, 1.11.2003, p. 38) as amended by Commission Decision 2004/414/EC (OJ No. L151, 30.4.2004, p. 62) (animal casings).

13.  Commission Decision 2003/863/EC (OJ No. L325, 12.12.2003, p. 46) (gelatine and collagen from the USA).

14.  Commission Regulation (EC) No. 2074/2005 (frogs' legs, snails, gelatine, raw materials for the production of gelatine, collagen and raw materials for the production of collagen) (see paragraph 16 of Part I).

Animal by-products

15.  Regulation (EC) No. 1774/2002 of the European Parliament and of the Council laying down health rules concerning animal by-products not intended for human consumption (OJ No. L273, 10.10.2002, p. 1) as last amended by Commission Regulation (EC) No. 208/2006 (OJ No. L36, 8.2.2006, p. 25), and as read with Commission Decision 2005/760/EC (OJ No. L285, 28.10.2005 p. 60) as last amended by Commission Decision 2006/522/EC (OJ No. L205, 27.7.2006, p. 28).

16.  Regulation (EC) No. 878/2004 laying down transitional measures in accordance with Regulation (EC) No. 1774/2002 for certain animal by-products classified as Category 1 and 2 materials and intended for technical purposes (OJ No. L162, 30.4.2004, p. 62).

17.  Commission Decision 2004/407/EC on transitory and certification rules under Regulation (EC) No. 1774/2002 of the European Parliament and of the Council as regards import from certain third countries of photographic gelatine (OJ No. L151, 30.4.2004, p. 11) as amended by Commission Decision 2006/311/EC (OJ No. L115, 28.4.2006, p. 115).

18.  Commission Decision 2006/7/EC concerning certain protection measures in relation to the import of feathers from certain third countries (OJ No. L5, 10.1.2006, p. 17) as last amended by Commission Decision 2006/892/EC (OJ No. L343, 8.12.2006, p. 99).

Hay and straw (third countries from which imports are permitted)

19.  Commission Regulation (EC) No. 136/2004 laying down procedures for veterinary checks at Community border inspection posts on products imported from third countries (OJ No. L21, 28.1.2004, p. 11).

PART IX GENETIC MATERIAL

Bovine material

1.  Council Directive 88/407/EEC laying down the animal health requirements applicable to intra-Community trade in and imports of semen of domestic animals of the bovine species, (OJ No. L194, 22.7.88, p. 10) as last amended by Commission Decision 2006/16/EC (OJ No. L11, 17.1.2006, p. 21).

2.  Council Directive 89/556/EEC on animal health conditions governing intra-Community trade in and importation from third countries of embryos of domestic animals of the bovine species (OJ No. L302, 19.10.89, p. 1) as last amended by Commission Decision 2006/60/EC (OJ No. L31, 3.2.2006, p. 24).

3.  Commission Decision 92/452/EEC establishing lists of embryo collection teams approved in third countries for export of bovine embryos to the Community (OJ No. L250, 29.8.92 p. 40) as last amended by Commission Decision 2006/556/EC (OJ No. L218, 9.8.2006, p. 20).

4.  Commission Decision 2004/639/EC laying down the importation conditions of semen of domestic animals of the bovine species (OJ No. L292, 15.9.2004, p. 21), as last amended by Commission Decision 2006/292/EC (OJ No. L107, 20.4.2006, p. 42).

5.  Commission Decision 2006/168/EC establishing the animal health and veterinary certification requirements for imports into the Community of bovine embryos and repealing Commission Decision 2005/217/EC (OJ No. L57, 28.2.2006, p. 19).

Porcine material

6.  Council Directive 90/429/EEC laying down the animal health requirements applicable to intra-Community trade in and imports of semen of domestic animals of the porcine species (OJ No. L224, 18.8.90, p. 62) as last amended by the Act of Accession (see paragraph 3 of Part V).

7.  Commission Decision 93/160/EEC drawing up a list of third countries from which member States authorize the importation of semen of domestic animals of the porcine species (OJ No. L67, 19.3.93 p. 27).

8.  Commission Decision 94/63/EC drawing up a provisional list of third countries from which member States authorize imports of semen, ova and embryos of the ovine, caprine and equine species, ova and embryos of the porcine species (OJ No. L28, 2.2.94, p. 47) as last amended by Commission Decision 2004/211/EC (OJ No. L73, 11.3.2004, p. 1).

9.  Commission Decision 2002/613/EC laying down the importation conditions of semen of domestic animals of the porcine species (OJ No. L196, 25.7.2002, p. 45) as last amended by Commission Decision 2006/271/EC (OJ No. L99, 7.4.2006, p. 29).

Ovine and caprine material

10.  Council Directive 92/65/EEC laying down animal health requirements governing trade in and imports into the Community of animals, semen, ova and embryos not subject to animal health requirements laid down in specific Community rules referred to in Annex A (I) to Directive 90/425/EEC, (OJ No. L268, 14.9.92, p. 54) as last amended by Commission Decision 2005/64/EC (OJ No. L27, 29.1.2005, p. 48).

11.  Commission Decision 94/63/EC (see paragraph 8 of this Part).

Equine material

12.  Council Directive 92/65/EEC (see paragraph 10 of this Part).

13.  Commission Decision 96/539/EC on animal health requirements and veterinary certification for imports into the Community of semen of the equine species, (OJ No. L230, 11.9.96, p. 23) as last amended by the Act of Accession (see paragraph 3 of Part V).

14.  Commission Decision 96/540/EC on animal health requirements and veterinary certification for imports into the Community of ova and embryos of the equine species (OJ No. L230, 11.9.96, p. 28) as amended by the Act of Accession (see paragraph 3 of Part V).

15.  Commission Decision 2004/211/EC establishing the list of third countries and parts of territory thereof from which member States authorise import of live equidae and semen, ova and embryos of the equine species, and amending Decisions 93/195/EC and 94/63/EC (OJ No. L73, 11.3.2004, p. 1).

16.  Commission Decision 2004/616/EC establishing the list of approved semen collection centres for imports of equine semen from third countries (OJ No. L278, 27.8.2004, p. 64).

Fish material

17.  Council Directive 91/67/EEC concerning the animal health conditions governing the placing on the market of aquaculture animals and products (OJ No. L46, 19.2.91, p. 1), as last amended by Council Regulation (EC) No. 806/2003 (OJ No. L122, 16.5.2003, p. 1).

PART X FISHERY PRODUCTS

General provisions

1.  Council Directive 91/67/EEC (see paragraph 17 of Part IX).

2.  Commission Decision 93/140/EEC laying down the detailed rules relating to the visual inspection for the purpose of detecting parasites in fishery products (OJ No. L56, 9.3.93, p. 42).

3.  Commission Decision 94/356/EC laying down detailed rules for the application of Council Directive 91/493/EEC as regards own health checks on fishery products (OJ No. L156, 23.6.94, p. 50).

4.  Commission Decision 95/149/EC fixing total volatile basic nitrogen (TVB-N) limit values for certain categories of fishery products and specifying the analysis methods to be used (OJ No. L97, 29.4.95, p. 84).

5.  Commission Directive 2001/22/EC laying down the sampling methods and the methods of analysis for the official control of the levels of lead, cadmium, mercury and 3-MCPD in foodstuffs (OJ No. L77, 16.3.2001, p. 14) as corrected by Commission Decision 2001/873/EC (OJ No. L325, 8.12.2001, p. 34).

6.  Commission Decision 2003/774/EC approving certain treatments to inhibit the development of pathogenic micro-organisms in bivalve molluscs and marine gastropods (OJ No. L283, 31.10.2003, p. 78).

7.  Commission Decision 2003/804/EC laying down the animal health conditions and certification requirements for imports of molluscs, their eggs and gametes for further growth, fattening, relaying or human consumption (OJ No. L302, 20.11.2003, p. 22) as last amended by Commission Decision 2005/409/EC (OJ No. L139, 2.6.2005, p. 16).

8.  Commission Decision 2003/858/EC laying down the animal health conditions and certification requirements for imports of live fish, their eggs and gametes intended for farming, live fish of aquaculture origin and products thereof intended for human consumption (OJ No. L324, 11.12.2003, p. 37) as last amended by Commission Decision 2005/742/EC (OJ No. L279, 22.10.2005, p. 71).

9.  Commission Decision 2004/453/EC implementing Council Directive 91/67/EC as regards measures against certain diseases in aquaculture animals (OJ No. L156, 30.4.2004, p. 5).

Health certification

10.  Commission Decision 95/328/EC establishing health certification for fishery products from third countries which are not yet covered by a specific Decision (OJ No. L191, 12.8.95, p. 32) as last amended by Commission Decision 2004/109/EC (OJ No. L32, 5.2.2004, p. 17).

11.  Commission Decision 96/333/EC establishing health certification of live bivalve molluscs, echinoderms, tunicates and marine gastropods from third countries which are not covered by a specific Decision (OJ No. L127, 25.5.96, p. 33) as last amended by Commission Decision 2004/119/EC (OJ No. L36, 7.2.2004, p. 56).

12.  Commission Decision 98/418/EC (OJ No. L190, 4.7.98, p. 53) (Uganda, Tanzania, Kenya and Mozambique).

13.  Commission Decision 2000/127/EC (OJ No. L36, 11.2.2000, p. 43) (Tanzania).

14.  Commission Decision 2003/804/EC (see paragraph 8 of this Part).

15.  Commission Decision 2003/858/EC (see paragraph 9 of this Part).

Third country equivalence

16.  Commission Decision 97/20/EC establishing the list of third countries fulfilling the equivalence conditions for the production and placing on the market of bivalve molluscs, echinoderms, tunicates and marine gastropods (OJ No. L6, 10.1.97, p. 46) as last amended by Commission Decision 2002/469/EC (OJ No. L163, 21.6.2002, p. 16).

Third countries from which fishery products may be imported

17.  Commission Decision 97/296/EC drawing up a list of third countries from which the import of fishery products is authorised for human consumption (OJ No. L122, 14.5.97, p. 21), as last amended by Commission Decision 2006/200/EC (OJ No. L171, 10.3.2006, p. 50).

Third country establishments from which fishery products may be imported

18.  Regulation (EC) No. 854/2004 (see paragraph 13 of Part I).

Special import conditions for fishery products

19.  Albania— Commission Decision 95/90/EC (OJ No. L70, 30.3.95, p. 27) as last amended by Commission Decision 95/235/EC (OJ No. L156, 7.7.95, p. 82).

20.  Algeria— Commission Decision 2005/498/EC (OJ No. L183, 14.7.2005, p. 92).

21.  Antigua and Barbuda— Commission Decision 2005/72/EC (OJ No. L28, 1.2.2005, p. 49).

22.  Argentina— Commission Decision 93/437/EC (OJ No. L202, 12.8.93, p. 42), as last amended by Commission Decision 97/276/EC (OJ No. L108, 25.4.97, p. 53).

23.  Australia— Commission Decision 97/426/EC (OJ No. L183, 11.7.97, p. 21) as amended by Commission Decision 99/403/EC (OJ No. L151, 18.6.99, p. 35).

24.  Bahamas— Commission Decision 2005/499/EC (OJ No. L183, 14.7.2005, p. 99).

25.  Bangladesh— Commission Decision 98/147/EC (OJ No. L46, 17.2.98, p. 13).

26.  Belize— Commission Decision 2003/759/EC (OJ No. L273, 24.10.2003, p. 18).

27.  Brazil— Commission Decision 94/198/EC (OJ No. L93, 12.4.94, p. 26) as last amended by Commission Decision 96/193/EC (OJ No. L61, 12.3.96, p. 43).

28.  Bulgaria— Commission Decision 2002/472/EC (OJ No. L163, 21.6.2002, p. 24), as amended by Commission Decision 2005/497/EC (OJ No. L183, 14.7.2005, p. 88).

29.  Canada— Commission Decision 93/495/EC (OJ No. L232, 15.9.93, p. 43) as last amended by Commission Decision 2000/659/EC (OJ No. L276, 28.10.2000, p. 81).

30.  Cape Verde— Commission Decision 2003/763/EC (OJ No. L273, 24.10.2003, p. 38).

31.  Chile— Commission Decision 93/436/EC (OJ No. L202, 12.8.93, p. 31) as last amended by Commission Decision 2000/61/EC (OJ No. L22, 27.1.2000, p. 62).

32.  China— Commission Decision 2000/86/EC (OJ No. L26, 2.2.2000, p. 26) as last amended by Commission Decision 2005/572/EC (OJ No. L193, 23.7.2005, p. 37).

33.  Colombia— Commission Decision 94/269/EC (OJ No. L115, 6.5.94, p. 38) as last amended by Commission Decision 99/486/EC (OJ No. L190, 23.7.99, p. 32).

34.  Costa Rica— Commission Decision 2002/854/EC (OJ No. L301, 5.11.2002, p. 1).

35.  Croatia— Commission Decision 2002/25/EC (OJ No. L11, 15.1.2002, p. 25).

36.  Cuba— Commission Decision 98/572/EC (OJ No. L277, 14.10.98, p. 44).

37.  Egypt— Commission Decision 2004/38/EC (OJ No. L8, 14.1.2004, p. 17).

38.  Ecuador— Commission Decision 94/200/EC (OJ No. L93, 12.4.94, p. 34) as last amended by Commission Decision 96/31/EC (OJ No. L9, 12.1.96, p. 6).

39.  El Salvador— Commission Decision 2005/74/EC (OJ No. L28, 1.2.2005, p. 59).

40.  Falkland Islands— Commission Decision 98/423/EC (OJ No. L190, 4.7.98, p. 76).

41.  French Polynesia— Commission Decision 2003/760/EC (OJ No. L273, 24.10.2003, p. 23), as amended by Commission Decision 2005/154/EC (OJ No. L51, 24.2.2005, p. 19).

42.  Gabon— Commission Decision 2002/26/EC (OJ No. L11, 15.1.2002, p. 31).

43.  Gambia— Commission Decision 96/356/EC (OJ No. L137, 8.6.96, p. 31).

44.  Ghana— Commission Decision 98/421/EC (OJ No. L190, 4.7.98, p. 66).

45.  Greenland— Commission Decision 2002/856/EC (OJ No. L301, 5.11.2002, p. 11).

46.  Grenada— Commission Decision 2005/500/EC (OJ No. L183, 14.7.2005, p. 104).

47.  Guatemala— Commission Decision 98/568/EC (OJ No. L277, 14.10.98, p. 26) as amended by Commission Decision 99/487/EC (OJ No. L190, 23.7. 99, p. 36).

48.  Guinea— Commission Decision 2001/634/EC (OJ No. L221, 17.8.2001, p. 50) as amended by Commission Decision 2002/61/EC (OJ No. L24, 26.1.2002, p. 59).

49.  Guyana— Commission Decision 2004/40/EC (OJ No. L8, 14.1.2004, p. 27).

50.  Honduras— Commission Decision 2002/861/EC (OJ No. L301, 5.11.2002, p. 43).

51.  Hong Kong— Commission Decision 2005/73/EC (OJ No. L28, 1.2.2005, p. 54).

52.  India— Commission Decision 97/876/EC (OJ No. L356, 31.12.97, p. 57).

53.  Indonesia— Commission Decision 94/324/EC (OJ No. L145, 10.6.94, p. 23) as last amended by Commission Decision 2001/254/EC (OJ No. L91, 31.3.2001, p. 85).

54.  Iran— Commission Decision 2000/675/EC (OJ No. L280, 4.11.2000, p. 63).

55.  Ivory Coast— Commission Decision 96/609/EC (OJ No. L269, 22.10.96, p. 37), as amended by Commission Decision 2005/514/EC (OJ No. L187, 19.7.2005, p. 25).

56.  Jamaica— Commission Decision 2001/36/EC (OJ No. L10, 13.1.2001, p. 59).

57.  Japan— Commission Decision 95/538/EC (OJ No. L304, 16.12.95, p. 52) as amended by Commission Decision 2002/471/EC (OJ No. L163, 21.6.2002, p. 21).

58.  Kazakhstan— Commission Decision 2002/862/EC (OJ No. L301, 5.11.2002, p. 48) as last amended by Commission Decision 2003/905/EC (OJ No. L340, 24.12.2003, p. 74).

59.  Kenya— Commission Decision 2004/39/EC (OJ No. L8, 14.1.2004, p. 22).

60.  Korea, Republic of — Commission Decision 95/454/EC (OJ No. L264, 7.11.95, p. 37) as last amended by Commission Decision 2001/818/EC (OJ No. L307, 24.11.2001, p. 20).

61.  Madagascar— Commission Decision 97/757/EC (OJ No. L307, 12.11.97, p. 33), as amended by Commission Decision 2005/496/EC (OJ No. L183, 14.7.2005, p. 84).

62.  Malaysia— Commission Decision 96/608/EC (OJ No. L269, 22.10.96, p. 32).

63.  Maldives— Commission Decision 98/424/EC (OJ No. L190, 4.7.98, p. 81) as amended by Commission Decision 2001/252/EC (OJ No. L91, 31.3.2001, p. 78).

64.  Mauritania— Commission Decision 96/425/EC (OJ No. L175, 13.7.96, p. 27).

65.  Mauritius— Commission Decision 99/276/EC (OJ No. L108, 27.4.99, p. 52) as amended by Commission Decision 2000/84/EC (OJ No. L26, 2.2.2000, p. 18).

66.  Mayotte— Commission Decision 2003/608/EC (OJ No. L210, 20.08.2003 p. 25).

67.  Mexico— Commission Decision 98/695/EC (OJ No. L332, 8.12.98, p. 9) as last amended by Commission Decision 2005/70/EC (OJ No. L28, 1.2.2005, p. 41).

68.  Morocco— Commission Decision 95/30/EC (OJ No. L42, 24.2.95, p. 32) as last amended by Commission Decision 2004/367/EC (OJ No. L114, 21.4.2004, p. 36).

69.  Mozambique— Commission Decision 2002/858/EC (OJ No. L301, 5.11.2002, p. 24).

70.  Namibia— Commission Decision 2000/673/EC (OJ No. L280, 4.11.2000, p. 52).

71.  Netherlands Antilles— Commission Decision 2003/762/EC (OJ No. L273, 24.10.2003, p. 33).

72.  New Caledonia— Commission Decision 2002/855/EC (OJ No. L301, 5.11.2002, p. 6).

73.  New Zealand— Commission Decision 94/448/EC (OJ No. L184, 20.7.94, p. 16) as last amended by Commission Decision 99/402/EC (OJ No. L151, 18.6.99, p. 31).

74.  Nicaragua— Commission Decision 2001/632/EC (OJ No. L221, 17.8.2001, p. 40).

75.  Nigeria— Commission Decision 98/420/EC (OJ No. L190, 4.7.98, p. 59).

76.  Oman— Commission Decision 99/527/EC (OJ No. L203, 3.8.99, p. 63).

77.  Pakistan— Commission Decision 2000/83/EC (OJ No. L26, 2.2.2000, p. 13).

78.  Papua New Guinea— Commission Decision 2002/859/EC (OJ No. L301, 5.11.2002, p. 33).

79.  Panama— Commission Decision 99/526/EC (OJ No. L203, 3.8.99, p. 58).

80.  Peru— Commission Decision 95/173/EC (OJ No. L116, 23.5.95, p. 41) as amended by Commission Decision 95/311/EC (OJ No. L186, 5.8.95, p. 78).

81.  Philippines— Commission Decision 95/190/EC (OJ No. L123, 3.6.95, p. 20) as amended by Commission Decision 96/256/EC (OJ No. L86, 4.4.96, p. 83).

82.  Romania— Commission Decision 2004/361/EC (OJ No. L113, 20.4.2004, p. 54).

83.  Russia— Commission Decision 97/102/EC (OJ No. L35, 5.2.97, p. 23) as last amended by Commission Decision 2005/155/EC (OJ No. L51, 24.2.2005, p. 23).

84.  Saint Pierre et Miquelon— Commission Decision 2003/609/EC (OJ No. L210, 20.8.2003, p. 30).

85.  Saudi Arabia— Commission Decision 2005/218/EC (OJ No. L69, 16.3.2005, p. 50).

86.  Senegal— Commission Decision 96/355/EC (OJ No. L137, 8.6.96, p. 24).

87.  Serbia and Montenegro— Commission Decision 2004/37/EC (OJ No. L8, 14.1.2004, p. 12).

88.  Seychelles— Commission Decision 99/245/EC (OJ No. L91, 7.4.99, p. 40).

89.  Singapore— Commission Decision 94/323/EC (OJ No. L145, 10.6.94, p. 19) as last amended by Commission Decision 2000/660/EC (OJ No. L276, 28.10.2000, p. 85).

90.  South Africa— Commission Decision 96/607/EC (OJ No. L269, 22.10.96, p. 23).

91.  Sri Lanka— Commission Decision 2003/302/EC (OJ No. L110, 03.05.2003, p. 6).

92.  Suriname— Commission Decision 2002/857/EC (OJ No. L301, 5.11.2002, p. 19).

93.  Switzerland— Commission Decision 2002/860/EC (OJ No. L301, 5.11.2002, p. 38).

94.  Taiwan— Commission Decision 94/766/EC (OJ No. L305, 30.11.94, p. 31) as last amended by Commission Decision 99/529/EC (OJ No. L203, 3.8.99, p. 73).

95.  Tanzania— Commission Decision 98/422/EC (OJ No. L190, 4.7.98, p. 71).

96.  Thailand— Commission Decision 94/325/EC (OJ No. L145, 10.6.94, p. 30) as last amended by Commission Decision 97/563/EC (OJ No. L232, 23.8.97, p. 12).

97.  Tunisia— Commission Decision 98/570/EC (OJ No. L277, 14.10.98, p. 36) as last amended by Commission Decision 2002/819/EC (OJ No. L281, 19.10.2002, p. 18).

98.  Turkey— Commission Decision 2002/27/EC (OJ No. L11, 15.1.2002, p. 36).

99.  Uganda— Commission Decision 2001/633/EC (OJ No. L221, 17.8.2001, p. 45).

100.  United Arab Emirates— Commission Decision 2003/761/EC (OJ No. L273, 24.10.2003, p. 28).

101.  United States of America— Commission Decision 2006/199/EC (OJ No. L71, 10.3.2006, p. 17).

102.  Uruguay— Commission Decision 96/606/EC (OJ No. L269, 22.10.96, p. 18) as amended by Commission Decision 2002/20/EC (OJ No. L10, 12.1.2002, p. 75).

103.  Venezuela— Commission Decision 2000/672/EC (OJ No. L280, 4.11.2000, p. 46) as amended by Commission Decision 2002/833/EC (OJ No. L285, 23.10.2002, p. 22).

104.  Vietnam— Commission Decision 99/813/EC (OJ No. L315, 9.12.99, p. 39) as last amended by Commission Decision 2004/267/EC (OJ No. L83, 20.3.2004, p. 26).

105.  Yemen— Commission Decision 99/528/EC (OJ No. L203, 3.8.99, p. 68).

106.  Zimbabwe— Commission Decision 2004/360/EC (OJ No. L113, 20.4.2004, p. 48).

Special import conditions for bivalve molluscs

107.  Australia— Commission Decision 97/427/EC (OJ No. L183, 11.7.97, p. 38) as amended by Commission Decision 99/531/EC (OJ No. L203, 3.8.99, p. 77).

108.  Chile— Commission Decision 96/675/EC (OJ No. L313, 3.12.96, p. 38).

109.  Japan— Commission Decision 2002/470/EC (OJ No. L163, 21.6.2002, p. 19).

110.  Jamaica— Commission Decision 2001/37/EC (OJ No. L10, 13.1.2001, p. 64).

111.  Korea, Republic of— Commission Decision 95/453/EC (OJ No. L264, 7.11.95, p. 35) as last amended by Commission Decision 2001/676/EC (OJ No. L236, 5.9.2001, p. 18).

112.  Morocco— Commission Decision 93/387/EC (OJ No. L166, 8.7.93, p. 40) as last amended by Commission Decision 96/31/EC (OJ No. L9, 12.1.96, p. 6).

113.  Peru— Commission Decision 2004/30/EC (OJ No. L6, 10.1.2004, p. 53).

114.  Thailand— Commission Decision 97/562/EC (OJ No. L232, 23.8.97, p. 9).

115.  Tunisia— Commission Decision 98/569/EC (OJ No. L277, 14.10.98, p. 31) as amended by Commission Decision 2002/819/EC (OJ No. L281, 19.10.2002, p. 18).

116.  Turkey— Commission Decision 94/777/EC (OJ No. L312, 6.12.94, p. 35) as last amended by Commission Decision 99/767/EC (OJ No. L302, 25.11.99, p. 26).

117.  Uruguay— Commission Decision 2002/19/EC (OJ No. L10, 12.1.2002, p. 73).

118.  Vietnam— Commission Decision 2000/333/EC (OJ No. L114, 13.5.2000, p. 42) as amended by Commission Decision 2004/263/EC (OJ No. L81, 19.3.2004, p. 88).

Regulation 8(4)(b)

SCHEDULE 2

Equivalence Decisions

1.  Council Decision 1999/201/EEC on the conclusion of the Agreement between the European Community and the Government of Canada on sanitary measures to protect public and animal health in respect of trade in live animals and animal products (OJ No. L71, 18.3.1999, p. 1).

2.  Council Decision 97/132/EC on the conclusion of the Agreement between the European Community and New Zealand on sanitary measures applicable to trade in live animals and animal products (OJ No. L57, 26.2.97, p. 4) as last amended by Commission Decision 2004/751/EC (OJ No. L332, 6.11.2004, p. 16).

3.  Council Decision 2002/957/EC on the conclusion of an Agreement in the form of Exchange of Letters concerning the amendment to the Annexes to the Agreement between the European Community and New Zealand on sanitary measures applicable to trade in live animals and animal products (OJ No. L333, 10.12.2002, p. 13).

4.  Commission Decision 2003/56/EC (see paragraph 7 of Part I of Schedule 1).

5.  Council and Commission Decision 2002/309/EC on the conclusion of an Agreement between the European Community and the Swiss Confederation on Trade in Agricultural Products (OJ No. L114, 30.4.2002, p. 1, with the full text of the Agreement at p. 132) as last amended by Commission Decision 2005/962/EC (OJ No. L347, 30.12.2005, p. 93).

Regulations 54, 55 and 56

SCHEDULE 3 Calculation of Charges for Veterinary Checks

PART 1 COSTS COVERED BY THE CHARGES

1.  For the purposes of this Schedule, “the actual cost” (“cost wirioneddol”), in relation to veterinary checks carried out on a consignment at a border inspection post, means the aggregate of—

(a) the proportion properly attributable to those veterinary checks of the cost of any items listed in paragraph 2 which relate partly to those veterinary checks; and

(b) the full cost of any items listed in paragraph 2 which relate wholly to those veterinary checks.

2.  The items referred to in paragraph 1 are the following—

(a) the salaries and fees, together with overtime payments and employers' national insurance and superannuation contributions, of all staff directly involved in carrying out veterinary checks, and of all staff engaged in the management or administration of veterinary checks, at the border inspection post;

(b) recruiting and training the staff referred to in item (a);

(c) travel and related incidental expenses incurred in carrying out the veterinary checks, except where incurred by a person attending his or her normal place of work;

(d) office accommodation, equipment and services for staff involved in carrying out veterinary checks at the border inspection post, including depreciation of office furniture and equipment and the cost of information technology, stationery and forms;

(e) protective clothing and equipment used in carrying out the veterinary checks;

(f) laundering the protective clothing referred to in item (e);

(g) sampling, testing and analysing samples (except sampling and testing for the presence of salmonella in processed animal protein not intended for human consumption);

(h) routine invoicing and collection of charges for veterinary checks at the border inspection posts; and

(i) providing payroll and personnel services in connection with the employment of staff carrying out veterinary checks at the border inspection post.

PART II CONSIGNMENTS FROM NEW ZEALAND

The charge for veterinary checks carried out on a consignment brought into the customs territory of the Community from New Zealand is 1.5 euro for each tonne of the consignment, subject to a minimum of 30 euro and a maximum of 350 euro, save that where the actual cost of the veterinary checks carried out on a consignment exceeds 350 euro, the amount of the charge is the actual cost.

PART III MEAT AND MEAT PRODUCTS

The charge for veterinary checks carried out on a consignment (other than a consignment to which Part II applies) covered by—

(a) Chapter III of Council Directive 71/118/EEC on health problems affecting trade in fresh poultrymeat (OJ No. L55, 8.3.71, p. 23) as amended and updated by Council Directive 92/116/EEC (OJ No. L62, 15.3.93, p. 1) and last amended by the Act of Accession (see paragraph 3 of Part V of Schedule 1);

(b) Council Directive 72/462/EEC on health and veterinary inspection problems upon importation of bovine animals and swine and fresh meat or meat products from third countries (OJ No. L302, 31.12.72, p.28), as last amended by Council Regulation (EC) No. 1452/2001, OJ No. L198, 21.7.2001, p 11);

(c) Chapter III of Council Directive 92/45/EEC on public health and animal health problems relating to the killing of wild game and the placing on the market of the wild game meat (OJ No. L268, 14.9.92, p 35) as last amended by the Act of Accession (see paragraph 3 of Part V of Schedule 1); or

(d) Chapter 11 of Annex I to Council Directive 92/118/EEC laying down animal health and public health requirements governing trade in and imports into the Community of products not subject to the said requirements laid down in specific Community rules referred to in Annex A(1) to Directive 89/662/EEC and, as regards pathogens, to Directive 90/425/EEC, as last amended by Commission Regulation (EC) No. 445/2004 (OJ No. L72, 11.3.2004, p. 60),

is—

(i) 30 euro;

(ii) 5 euro per tonne of the consignment; or

(iii) the actual cost of the veterinary checks carried out on the consignment,

whichever is the greatest.

PART IV FISHERY PRODUCTS

The charge for veterinary checks carried out on a consignment of fishery products falling under Chapter II of Council Directive 91/493/EEC laying down the health conditions for the production and the placing on the market of fishery products (OJ No. L268, 24.9.91, p. 15) as last amended by the Act of Accession (see paragraph 3 of Part V of Schedule 1), other than a consignment to which Part II applies is—

(a) 30 euro;

(b) 5 euro per tonne of the consignment for the first 100 tonnes plus—

(i) 1.5 euro per additional tonne if the consignment has undergone no preparation other than gutting; or

(ii) 2.5 euro per additional tonne in other cases; or

(c) the actual cost of the veterinary checks carried out on the consignment,

whichever is the greatest.

PART V ALL OTHER PRODUCTS

The charge for veterinary checks carried out on a consignment, other than a consignment to which Part II, III or IV applies, is the actual cost of the veterinary checks carried out on the consignment.

Regulation 63

SCHEDULE 4 Provisions Where Due Diligence Defence is Available

• Paragraph (4) of regulation 4 (Exemption for authorised products and personal imports);

• Regulation 15 (Prohibition of non-conforming products);

• Paragraphs (1) and (2) of regulation 16 (Prohibition of introduction of products except at border inspection posts);

• Regulation 17 (Advance notice of introduction or presentation);

• Paragraphs (1) and (2) of regulation 18 (Presentation of products at border inspection posts);

• Paragraph (1) of regulation 20 (Common veterinary entry document to accompany consignment);

• Paragraph (2) of regulation 29 (Disposal of unused catering supplies);

• Paragraphs (3) and (4) of regulation 37 (Products transported under supervision);

• Paragraphs (2), (5) and (6) of regulation 38 (Transhipment of products intended for import);

• Regulation 40 (Prior authorisation of transit);

• Paragraphs (2)(a) and (c) of regulation 42 (Movement of transit products);

• Paragraph (1) of regulation 45 (Additional information to be given in advance);

• Paragraph (3) of regulation 53 (Movement of returned products).

Explanatory Note

(This note is not part of the Regulations)

These Regulations revoke and re-enact with changes the Products of Animal Origin (Third Country Imports) (Wales) Regulations 2005 (S.I. 2005/666). The principal changes are to regulations 5, 17, 48 and 49 (see below), and to Schedules 1 and 3, which have been revised in order to implement Community instruments that have come into force since the Products of Animal Origin (Third Country Imports) (Wales) Regulations 2005 were made.

The Regulations implement for Wales Council Directive 97/78/EC (laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries) (OJ No. L24, 30.1.98, p. 9). Commission Decision 2002/349/EC (laying down the list of products to be examined at border inspection posts under Council Directive 97/78/EC) (OJ No. L121, 8.5.2002, p. 6) specifies the products of animal origin to which the Directive applies— meat, fish (including shellfish), milk, and products made from these, together with egg products and a large number of animal by-products, including casings, skins, bones and blood — from third countries.

The products to which the Regulations apply (defined in regulation 2) must comply with the requirements listed, by reference to the relevant Community legislation, in Schedule 1.

Regulation 4 provides for exemptions from Parts 3 to 9 of the Regulations. Regulation 4(7) provides that Part 3, with the exception of regulation 25, and Parts 4 to 9 do not apply to products intended for personal use that comply with the conditions laid down in that regulation.

Regulation 5 defines the authorities that enforce the Regulations. Usually, these will be port health authorities, who appoint official veterinary surgeons and official fish inspectors to conduct veterinary checks at each border inspection post in their area (regulation 6). Regulation 5 has been revised to include the provision that the Commissioners for Her Majesty’s Revenue and Customs enforce regulation 16 at points of entry other than border inspection posts. A further revision at regulation 5(4) amends enforcement provisions in relation to illegally imported products found inland so that local authority enforcement officers who are not authorised officers under the Regulations can take hold of any products of animal origin they suspect of having been illegally imported until an authorised officer can take charge of it. Regulation 5(9) creates a new offence relating to the unlawful disclosure of information received from Her Majesty’s Revenue and Customs.

Regulations 7, 8, 9 and 11 confer the necessary enforcement powers on the enforcement authorities. Regulation 13 has been revised to enable the approval of Border Inspection Posts to be suspended in part (previously only a full suspension of approval was permitted).

Part 3 establishes the inspection system that will apply to products in general. The bringing into Wales of products that do not comply with the Schedule 1 requirements is prohibited, unless they are being transported across Wales (regulation 15). Products must be brought in at border inspection posts, advance notice of their introduction must be given, and they must be made available for inspection, together with required documentation, at a border inspection post (regulations 16 to 19). Regulation 17 has been revised in order to bring requirements for pre-notification of imported consignments to Border Inspection Posts into line with Commission Regulation 136/2004 laying down procedures for veterinary checks at Community Border Inspection Posts on products imported from third countries. Regulations 21 to 28 deal with products that are rejected at inspection, are brought in illegally, or present a risk to animal health or public health.

Parts 4 to 8 lay down special provisions that apply to particular categories of product (on-board catering supplies, products intended for free circulation in the Community, products in transit across Wales, products intended for warehousing under particular Customs regimes, and products exported from the Community and then returned to it). Regulations 48 and 49 are new provisions, which implement procedures for the direct movement of consignments, intended as food for passengers or crew, that do not meet EU import requirements from Border Inspection Posts to ships operating internationally.

Part 9 deals with the calculation and payment of charges for the veterinary checks provided for in the Regulations; Part 10 confers on the National Assembly and the Food Standards Agency power to prohibit the bringing of products into Wales from non-EEA countries in which there is an outbreak of animal disease; Part 11 establishes offences and penalties; Part 12 deals with the service of notices and with notification of decisions; and Part 13 provides that certain existing provisions do not apply to products to which these Regulations apply, and revokes the Products of Animal Origin (Third Country Imports) (Wales) Regulations 2005. Part I of Schedule 3 has been amended in relation to Salmonella testing to enable Border Inspection Posts to charge for such tests carried out in accordance with Community legislation.

A regulatory appraisal of the effect which this instrument will have on the costs of business has been prepared and copies can be obtained from the National Assembly for Wales, Cathays Park, Cardiff CF10 3NQ.

(1)

S.I. 2005/2766.

(2)

1972 c. 68.

(3)

1973 c. 51.

(4)

OJ No. L69, 13.3.2003, p. 31.

(5)

OJ No. L136, 22.01.2004, p. 11.

(6)

OJ No. L302, 19.10.92, p. 1, as last amended by Council Regulation (EC) No. 648/2005 (OJ No. L117, 4.5.2005, p. 13).

(7)

OJ No. L326, 11.12.2001, p. 44, as last amended by Commission Decision 2006/414/EC (OJ No. L164, 16.6.2006, p. 27).

(8)

OJ No. L24, 30.1.98, p. 9, as last amended by Regulation (EC) No. 882/2004 of the European Parliament and of the Council (see Corrigendum OJ No. L191, 28.5.2004, p. 1).

(9)

OJ No. L46, 19.2.91, p. 1, as last amended by Council Regulation (EC) No. 806/2003 (OJ No. L122, 16.5.2003, p. 1).

(10)

OJ No. L139, 30.04.2004, p. 206, as amended by Corrigendum to Regulation (EC) No. 854/2004 (OJ No. L226, 25.06.2004, p. 83).

(11)

OJ No. L121, 8.5.2002, p. 6, as read with Commission Regulations (EC) No. 136/2004 (OJ No. L21, 28.1.2004, p. 11) and (EC) No. 745/2004 (OJ No. L122, 26.4.2004, p. 1).

(12)

OJ No. L273, 10.10.2002, p. 1, as last amended by Commission Regulation (EC) No. 208/2006 (OJ No. L36, 8.2.2006, p. 25) and as read with Commission Regulations (EC) No. 811/2003, 812/2003 and 813/2003 (OJ No. L117, 13.5.2003, p. 14, p. 19 and p. 22), Commission Decisions 2003/320/EC, 2003/321/EC, 2003/326/EC and 2003/327/EC (OJ No. L117, 13.5.2003, p. 24, p. 30, p. 42 and p. 44) and Commission Regulation (EC) No. 780/2004 (OJ No. L123, 27.4.2004, p. 64).

(13)

OJ No. L21, 28.1.2004, p. 11.

(14)

S.I. 2006/1293 (W.127).

(15)

S.I.2006/31 (W.5).

(16)

OJ No. L306, 23.11.2001, p. 28.

(17)

1979 c. 2, as amended by S.I. 1992/3095.

(18)

OJ No. L 165, 30.4.2004, p. 1, as amended by Corrigendum OJ No. L 191, 28.5.2004, p. 1.

(19)

1980 c. 43.

(20)

S.I. 2006/1293 (W. 127).

(21)

OJ No. L224, 18.8.90, p. 1, as last amended by Commission Regulation (EC) No. 1451/2006 (OJ No. L271, 30.9.2006, p.37).

(22)

OJ No. L125, 23.5.96, p. 10, as last amended by Council Regulation (EC) No. 882/2004 of the European Parliament and of the Council (see Corrigendum OJ No. L191, 28.5.2004, p. 1).

(23)

1979 c. 2, as amended by S.I. 1992/3095.

(24)

OJ No. L253, 11.10.93, p. 1, as last amended by Commission Regulation (EC) No. 402/2006 (OJ No. L070, 09.03.2006, p. 35).

(25)

OJ No. L240, 23.9.2000, p. 14.

(26)

OJ No. L378, 31.12.82, p. 58, as last amended by Commission Decision 2004/216/EC (OJ No. L67, 5.3.2004, p. 27).

(27)

S.I. 1980/12, as amended by S.I. 1984/1326, 1990/2371, and 1994/2920.

(28)

S.I. 1980/14, as amended by S.I. 1982/948, 1990/2371, 1994/2920 and 1994/3142, and as read with S.I. 1997/322.

(29)

S.I. 1984/1325, as amended by S.I. 1993/1966.

(30)

S.I. 1981/677, as amended by S.I. 1982/459 and S.I. 1990/2371.

(31)

S.I. 2005/666 (W.56), as amended by S.I. 2005/3395 (W. 271) and S.I. 2006/767 (W.74).

(32)

1998 c. 38.