http://www.legislation.gov.uk/eur/2012/528/article/3/2020-12-31Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (Text with EEA relevance)Regulation (EU) No 528/2012 of the European Parliament and of the CouncilRegulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (Text with EEA relevance)King's Printer of Acts of Parliamenthttps://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02012R0528-20191120texttext/xmlen2024-07-31Expert Participation2020-12-31 CHAPTER I<Strong>SCOPE AND DEFINITIONS</Strong>DefinitionsArticle 31For the purposes of this Regulation, the following definitions shall apply:a‘biocidal product’ meansany substance or mixture, in the form in which it is supplied to the user, consisting of, containing or generating one or more active substances, with the intention of destroying, deterring, rendering harmless, preventing the action of, or otherwise exerting a controlling effect on, any harmful organism by any means other than mere physical or mechanical action,any substance or mixture, generated from substances or mixtures which do not themselves fall under the first indent, to be used with the intention of destroying, deterring, rendering harmless, preventing the action of, or otherwise exerting a controlling effect on, any harmful organism by any means other than mere physical or mechanical action.A treated article that has a primary biocidal function shall be considered a biocidal product.b‘micro-organism’ means any microbiological entity, cellular or non-cellular, capable of replication or of transferring genetic material, including lower fungi, viruses, bacteria, yeasts, moulds, algae, protozoa and microscopic parasitic helminths;c‘active substance’ means a substance or a micro-organism that has an action on or against harmful organisms;d‘existing active substance’ means a substance which was on the market on 14 May 2000 , in a country which was a Member State of the EU on that date, as an active substance of a biocidal product for purposes other than scientific or product and process-orientated research and development;e‘new active substance’ means a substance which was not on the market on 14 May 2000 in a country which was a Member State of the EU on that date as an active substance of a biocidal product for purposes other than scientific or product and process-orientated research and development;f‘substance of concern’ means any substance, other than the active substance, which has an inherent capacity to cause an adverse effect, immediately or in the more distant future, on humans, in particular vulnerable groups, animals or the environment and is present or is produced in a biocidal product in sufficient concentration to present risks of such an effect.Such a substance would, unless there are other grounds for concern, normally be:...a substance classified as hazardous or that meets the criteria for classification as hazardous according to Regulation (EC) No 1272/2008, and that is present in the biocidal product at a concentration leading the product to be regarded as hazardous within the meaning of that Regulation,a substance which meets the criteria for being a persistent organic pollutant (POP) under Regulation (EC) No 850/2004, or which meets the criteria for being persistent, bio-accumulative and toxic (PBT) or very persistent and very bio-accumulative (vPvB) in accordance with Annex XIII to Regulation (EC) No 1907/2006;g‘harmful organism’ means an organism, including pathogenic agents, which has an unwanted presence or a detrimental effect on humans, their activities or the products they use or produce, on animals or the environment;h‘residue’ means a substance present in or on products of plant or animal origin, water resources, drinking water, food, feed or elsewhere in the environment and resulting from the use of a biocidal product, including such a substance’s metabolites, breakdown or reaction products;i‘making available on the market’ means any supply of a biocidal product or of a treated article for distribution or use in the course of a commercial activity, whether in return for payment or free of charge;j‘placing on the market’ means the first making available on the market of a biocidal product or of a treated article;k‘use’ means all operations carried out with a biocidal product, including storage, handling, mixing and application, except any such operation carried out with a view to exporting the biocidal product or the treated article outside Great Britain;l‘treated article’ means any substance, mixture or article which has been treated with, or intentionally incorporates, one or more biocidal products;m‘national authorisation’ means an administrative act by which the competent authority ... authorises the making available on the market and the use of a biocidal product or a biocidal product family ...;n‘Union authorisation’ means the administrative act by which the Commission authorised the making available on the market and use of a biocidal product or a product family in the territory of the Union or part thereof before IP completion day;o‘authorisation’ means national authorisation ... or authorisation in accordance with Article 26;p‘authorisation holder’ means the person established in the United Kingdom who is responsible for the placing on the market of a biocidal product in Great Britain and specified in the authorisation;q‘product-type’ means one of the product-types specified in Annex V;r‘single biocidal product’ means a biocidal product with no intended variations as to the percentage of the active or non-active substances it contains;s‘biocidal product family’ means a group of biocidal products having:similar uses;the same active substances;similar composition with specified variations; andsimilar levels of risk and efficacy;t‘letter of access’ means an original document, signed by the data owner or its representative, which states that the data may be used for the benefit of a third party by the competent authority for the purposes of this Regulation;u‘food’ and ‘feed’ mean food as defined in Article 2 of Regulation (EC) No 178/2002 and feed as defined in Article 3(4) of that Regulation;v. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .w‘technical equivalence’ means similarity, as regards the chemical composition and hazard profile, of a substance produced either from a source different to the reference source, or from the reference source but following a change to the manufacturing process and/or manufacturing location, compared to the substance of the reference source in respect of which the initial risk assessment was carried out, as established in Article 54;x. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .y‘advertisement’ means a means of promoting the sale or use of biocidal products by printed, electronic or other media;z‘nanomaterial’ means a natural or manufactured active substance or non-active substance containing particles, in an unbound state or as an aggregate or as an agglomerate and where, for 50 % or more of the particles in the number size distribution, one or more external dimensions is in the size range 1-100 nm.Fullerenes, graphene flakes and single-wall carbon nanotubes with one or more external dimensions below 1 nm shall be considered as nanomaterials.For the purposes of the definition of nanomaterial, ‘particle’, ‘agglomerate’ and ‘aggregate’ are defined as follows:‘particle’ means a minute piece of matter with defined physical boundaries,‘agglomerate’ means a collection of weakly bound particles or aggregates where the resulting external surface area is similar to the sum of the surface areas of the individual components,‘aggregate’ means a particle comprising strongly bound or fused particles;aa‘administrative change’ means an amendment of an existing authorisation of a purely administrative nature involving no change to the properties or efficacy of the biocidal product or biocidal product family;ab‘minor change’ means an amendment of an existing authorisation that is not of a purely administrative nature and requires only a limited re-assessment of the properties or efficacy of the biocidal product or biocidal product family;ac‘major change’ means an amendment of an existing authorisation which is neither an administrative change nor a minor change;ad‘vulnerable groups’ means persons needing specific consideration when assessing the acute and chronic health effects of biocidal products. These include pregnant and nursing women, the unborn, infants and children, the elderly and, when subject to high exposure to biocidal products over the long term, workers and residents;ae‘small and medium-sized enterprises’ or ‘SMEs’ means small and medium-sized enterprises as defined in Commission Recommendation 2003/361/EC of 6 May 2003 concerning the definition of micro, small and medium-sized enterprises.af‘the consent requirement’ means the requirement for consent in accordance with Article 83B;ag‘the UK List’ means the list of approved substances established and maintained in accordance with Article 8A;ah‘the Simplified Active Substance List’ means the list of active substances which can be used in biocidal products that qualify for the simplified authorisation procedure, established and maintained in accordance with Article 24A.ai“appropriate fee” means the fee payable for the activity concerned in regulations made under section 43 of the Health and Safety at Work etc. Act 1974 where the competent authority is appointed in accordance with regulation 5 of the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013;aj“Devolved Authority” means—ithe Scottish Ministers, oriithe Welsh Ministers.2For the purposes of this Regulation, the definitions laid down in Article 3 of Regulation (EC) No 1907/2006 shall apply for the following terms:a‘substance’;b‘mixture’;c‘article’;d‘product and process-orientated research and development’;e‘scientific research and development’.3The Secretary of State may issue a decision which is to be published, as to whether a substance is a nanomaterial, having regard in particular to Commission Recommendation 2011/696/EU of 18 October 2011 on the definition of nanomaterial and whether a specific product or group of products is a biocidal product or a treated article or neither.4A decision issued under paragraph 3 above is subject to the consent requirement.5The Secretary of State may by regulations adapt the definition of nanomaterial set out in point (z) of paragraph 1 of this Article in view of technical and scientific progress, taking into account the Recommendation referred to in paragraph 3 above.6Regulations made under paragraph 5 above are subject to the consent requirement.7Where any of the Devolved Authorities makes proposals in relation to adaptations under paragraph 5 above, the Secretary of State must have regard to such proposals in deciding whether to exercise functions in that paragraph. OJ L 124, 20.5.2003, p. 36. Substituted by Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market (Text with EEA relevance).Deleted by Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market (Text with EEA relevance).Art. 3(3)-(7) substituted for Art. 3(3) (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(3); 2020 c. 1, Sch. 5 para. 1(1)Art. 3(1)(af)-(aj) inserted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(k) (as amended by S.I. 2020/1567, reg. 1(2), Sch. 2 para. 23(d)); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(d) inserted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(a); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(e) inserted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(b); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(k) substituted (31.12.2020) by S.I. 2019/720, Sch. 2 para. 64(2)(d) (as substituted by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), reg. 1(2), Sch. 2 para. 23(a))Words in Art. 3(1)(m) omitted (31.12.2020) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(e)(i); 2020 c. 1, Sch. 5 para. 1(1)Art. 3(1)(n) substituted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(f) (as amended by S.I. 2020/1567, reg. 1(2), Sch. 2 para. 23(b)); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(o) omitted (31.12.2020) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(g); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(p) substituted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(h)(i); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(p) substituted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(h)(ii) (as amended by S.I. 2020/1567, reg. 1(2), Sch. 2 para. 23(c)); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(t) inserted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(i); 2020 c. 1, Sch. 5 para. 1(1)Art. 3(1)(x) omitted (31.12.2020) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(j); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(m) omitted (31.12.2020) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(e)(ii); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 3(1)(f) omitted (31.12.2020) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 64(2)(c); 2020 c. 1, Sch. 5 para. 1(1)
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<Number>CHAPTER I</Number>
<Title>
<Strong>SCOPE AND DEFINITIONS</Strong>
</Title>
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<Title>Definitions</Title>
<P1 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3" id="article-3">
<Pnumber>Article 3</Pnumber>
<P1para>
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<Pnumber PuncBefore="" PuncAfter=".">1</Pnumber>
<P2para>
<Text>For the purposes of this Regulation, the following definitions shall apply:</Text>
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<Text>‘biocidal product’ means</Text>
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<Para>
<Text>any substance or mixture, in the form in which it is supplied to the user, consisting of, containing or generating one or more active substances, with the intention of destroying, deterring, rendering harmless, preventing the action of, or otherwise exerting a controlling effect on, any harmful organism by any means other than mere physical or mechanical action,</Text>
</Para>
</ListItem>
<ListItem>
<Para>
<Text>any substance or mixture, generated from substances or mixtures which do not themselves fall under the first indent, to be used with the intention of destroying, deterring, rendering harmless, preventing the action of, or otherwise exerting a controlling effect on, any harmful organism by any means other than mere physical or mechanical action.</Text>
</Para>
</ListItem>
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<P3para>
<Text>A treated article that has a primary biocidal function shall be considered a biocidal product.</Text>
</P3para>
</P3>
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<Pnumber PuncBefore="(" PuncAfter=")">b</Pnumber>
<P3para>
<Text>‘micro-organism’ means any microbiological entity, cellular or non-cellular, capable of replication or of transferring genetic material, including lower fungi, viruses, bacteria, yeasts, moulds, algae, protozoa and microscopic parasitic helminths;</Text>
</P3para>
</P3>
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<Pnumber PuncBefore="(" PuncAfter=")">c</Pnumber>
<P3para>
<Text>‘active substance’ means a substance or a micro-organism that has an action on or against harmful organisms;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/d/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/d" id="article-3-1-d">
<Pnumber PuncBefore="(" PuncAfter=")">d</Pnumber>
<P3para>
<Text>
‘existing active substance’ means a substance which was on the market on 14 May 2000
<Addition ChangeId="key-079279b6dc84aef1ddedc2aef184bc04-1722007167002" CommentaryRef="key-079279b6dc84aef1ddedc2aef184bc04">, in a country which was a Member State of the EU on that date,</Addition>
as an active substance of a biocidal product for purposes other than scientific or product and process-orientated research and development;
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/e/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/e" id="article-3-1-e">
<Pnumber PuncBefore="(" PuncAfter=")">e</Pnumber>
<P3para>
<Text>
‘new active substance’ means a substance which was not on the market on 14 May 2000
<Addition ChangeId="key-9aae6502fa09e9593f160e229e195dd7-1722007167003" CommentaryRef="key-9aae6502fa09e9593f160e229e195dd7">in a country which was a Member State of the EU on that date</Addition>
as an active substance of a biocidal product for purposes other than scientific or product and process-orientated research and development;
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/f/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/f" id="article-3-1-f">
<Pnumber PuncBefore="(" PuncAfter=")">f</Pnumber>
<P3para>
<Text>‘substance of concern’ means any substance, other than the active substance, which has an inherent capacity to cause an adverse effect, immediately or in the more distant future, on humans, in particular vulnerable groups, animals or the environment and is present or is produced in a biocidal product in sufficient concentration to present risks of such an effect.</Text>
</P3para>
<P3para>
<Text>Such a substance would, unless there are other grounds for concern, normally be:</Text>
</P3para>
<P3para>
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<ListItem>
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<Text>
<CommentaryRef Ref="key-d2c824c8bb655b17dae9ea8f98e36cbb"/>
...
</Text>
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<Para>
<Text>a substance classified as hazardous or that meets the criteria for classification as hazardous according to Regulation (EC) No 1272/2008, and that is present in the biocidal product at a concentration leading the product to be regarded as hazardous within the meaning of that Regulation,</Text>
</Para>
</ListItem>
<ListItem>
<Para>
<Text>a substance which meets the criteria for being a persistent organic pollutant (POP) under Regulation (EC) No 850/2004, or which meets the criteria for being persistent, bio-accumulative and toxic (PBT) or very persistent and very bio-accumulative (vPvB) in accordance with Annex XIII to Regulation (EC) No 1907/2006;</Text>
</Para>
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</P3para>
</P3>
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<Pnumber PuncBefore="(" PuncAfter=")">g</Pnumber>
<P3para>
<Text>‘harmful organism’ means an organism, including pathogenic agents, which has an unwanted presence or a detrimental effect on humans, their activities or the products they use or produce, on animals or the environment;</Text>
</P3para>
</P3>
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<Pnumber PuncBefore="(" PuncAfter=")">h</Pnumber>
<P3para>
<Text>‘residue’ means a substance present in or on products of plant or animal origin, water resources, drinking water, food, feed or elsewhere in the environment and resulting from the use of a biocidal product, including such a substance’s metabolites, breakdown or reaction products;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/i/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/i" id="article-3-1-i">
<Pnumber PuncBefore="(" PuncAfter=")">i</Pnumber>
<P3para>
<Text>‘making available on the market’ means any supply of a biocidal product or of a treated article for distribution or use in the course of a commercial activity, whether in return for payment or free of charge;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/j/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/j" id="article-3-1-j">
<Pnumber PuncBefore="(" PuncAfter=")">j</Pnumber>
<P3para>
<Text>‘placing on the market’ means the first making available on the market of a biocidal product or of a treated article;</Text>
</P3para>
</P3>
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<Pnumber PuncBefore="(" PuncAfter=")">k</Pnumber>
<P3para>
<Text>
‘use’ means all operations carried out with a biocidal product, including storage, handling, mixing and application, except any such operation carried out with a view to exporting the biocidal product or the treated article outside
<Substitution ChangeId="key-041aa773d22be02ee7d09c8025e339d5-1722007167005" CommentaryRef="key-041aa773d22be02ee7d09c8025e339d5">Great Britain</Substitution>
;
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/l/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/l" id="article-3-1-l">
<Pnumber PuncBefore="(" PuncAfter=")">l</Pnumber>
<P3para>
<Text>‘treated article’ means any substance, mixture or article which has been treated with, or intentionally incorporates, one or more biocidal products;</Text>
</P3para>
</P3>
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<Pnumber PuncBefore="(" PuncAfter=")">m</Pnumber>
<P3para>
<Text>
‘national authorisation’ means an administrative act by which the competent authority
<CommentaryRef Ref="key-0c94da28836a7d27a4a884df261fd5c2"/>
... authorises the making available on the market and the use of a biocidal product or a biocidal product family
<CommentaryRef Ref="key-8d323ec30d9173ae28717d545691e89c"/>
...;
</Text>
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</Pnumber>
<P3para>
<Text>
<Substitution ChangeId="key-02fdc78c2e488e126ad2ea45edeb1a4d-1722007167009" CommentaryRef="key-02fdc78c2e488e126ad2ea45edeb1a4d">‘Union authorisation’ means the administrative act by which the Commission authorised the making available on the market and use of a biocidal product or a product family in the territory of the Union or part thereof before IP completion day;</Substitution>
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/o/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/o" id="article-3-1-o">
<Pnumber PuncBefore="(" PuncAfter=")">o</Pnumber>
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<Text>
‘authorisation’ means national authorisation
<CommentaryRef Ref="key-6f779ceee8ef57ddc03710443bf4e989"/>
... or authorisation in accordance with Article 26;
</Text>
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<Pnumber PuncBefore="(" PuncAfter=")">p</Pnumber>
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<Text>
‘authorisation holder’ means the person established
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who is responsible for the placing on the market of a biocidal product in
<Substitution ChangeId="key-67d8c02b194f8fb2047f182a9c8d0b73-1722007167013" CommentaryRef="key-67d8c02b194f8fb2047f182a9c8d0b73">Great Britain</Substitution>
and specified in the authorisation;
</Text>
</P3para>
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<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/q/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/q" id="article-3-1-q">
<Pnumber PuncBefore="(" PuncAfter=")">q</Pnumber>
<P3para>
<Text>‘product-type’ means one of the product-types specified in Annex V;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/r/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/r" id="article-3-1-r">
<Pnumber PuncBefore="(" PuncAfter=")">r</Pnumber>
<P3para>
<Text>‘single biocidal product’ means a biocidal product with no intended variations as to the percentage of the active or non-active substances it contains;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/s/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/s" id="article-3-1-s">
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<P3para>
<Text>
<Substitution ChangeId="O002001M002" CommentaryRef="c000001">‘biocidal product family’ means a group of biocidal products having:</Substitution>
</Text>
</P3para>
<P3para>
<OrderedList Type="roman" Decoration="parens">
<ListItem NumberOverride="(i)">
<Para>
<Text>
<Substitution ChangeId="O002001M002" CommentaryRef="c000001">similar uses;</Substitution>
</Text>
</Para>
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<Para>
<Text>
<Substitution ChangeId="O002001M002" CommentaryRef="c000001">the same active substances;</Substitution>
</Text>
</Para>
</ListItem>
<ListItem NumberOverride="(iii)">
<Para>
<Text>
<Substitution ChangeId="O002001M002" CommentaryRef="c000001">similar composition with specified variations; and</Substitution>
</Text>
</Para>
</ListItem>
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<Para>
<Text>
<Substitution ChangeId="O002001M002" CommentaryRef="c000001">similar levels of risk and efficacy;</Substitution>
</Text>
</Para>
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<Pnumber PuncBefore="(" PuncAfter=")">t</Pnumber>
<P3para>
<Text>
‘letter of access’ means an original document, signed by the data owner or its representative, which states that the data may be used for the benefit of a third party by
<Substitution ChangeId="key-c36c9df52a8d7f2e197162dc5bb09929-1722007167014" CommentaryRef="key-c36c9df52a8d7f2e197162dc5bb09929">the competent authority</Substitution>
for the purposes of this Regulation;
</Text>
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<Pnumber PuncBefore="(" PuncAfter=")">u</Pnumber>
<P3para>
<Text>‘food’ and ‘feed’ mean food as defined in Article 2 of Regulation (EC) No 178/2002 and feed as defined in Article 3(4) of that Regulation;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/v/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/v" id="article-3-1-v">
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v
</Pnumber>
<P3para>
<Text>. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .</Text>
</P3para>
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<Pnumber PuncBefore="(" PuncAfter=")">w</Pnumber>
<P3para>
<Text>‘technical equivalence’ means similarity, as regards the chemical composition and hazard profile, of a substance produced either from a source different to the reference source, or from the reference source but following a change to the manufacturing process and/or manufacturing location, compared to the substance of the reference source in respect of which the initial risk assessment was carried out, as established in Article 54;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/x/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/x" id="article-3-1-x">
<Pnumber PuncBefore="(" PuncAfter=")">
<CommentaryRef Ref="key-0045341a450f3705c91f61b32137f157"/>
x
</Pnumber>
<P3para>
<Text>. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/y/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/y" id="article-3-1-y">
<Pnumber PuncBefore="(" PuncAfter=")">y</Pnumber>
<P3para>
<Text>‘advertisement’ means a means of promoting the sale or use of biocidal products by printed, electronic or other media;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/z/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/z" id="article-3-1-z">
<Pnumber PuncBefore="(" PuncAfter=")">z</Pnumber>
<P3para>
<Text>‘nanomaterial’ means a natural or manufactured active substance or non-active substance containing particles, in an unbound state or as an aggregate or as an agglomerate and where, for 50 % or more of the particles in the number size distribution, one or more external dimensions is in the size range 1-100 nm.</Text>
</P3para>
<P3para>
<Text>Fullerenes, graphene flakes and single-wall carbon nanotubes with one or more external dimensions below 1 nm shall be considered as nanomaterials.</Text>
</P3para>
<P3para>
<Text>For the purposes of the definition of nanomaterial, ‘particle’, ‘agglomerate’ and ‘aggregate’ are defined as follows:</Text>
</P3para>
<P3para>
<UnorderedList Decoration="dash">
<ListItem>
<Para>
<Text>‘particle’ means a minute piece of matter with defined physical boundaries,</Text>
</Para>
</ListItem>
<ListItem>
<Para>
<Text>‘agglomerate’ means a collection of weakly bound particles or aggregates where the resulting external surface area is similar to the sum of the surface areas of the individual components,</Text>
</Para>
</ListItem>
<ListItem>
<Para>
<Text>‘aggregate’ means a particle comprising strongly bound or fused particles;</Text>
</Para>
</ListItem>
</UnorderedList>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/aa/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/aa" id="article-3-1-aa">
<Pnumber PuncBefore="(" PuncAfter=")">aa</Pnumber>
<P3para>
<Text>‘administrative change’ means an amendment of an existing authorisation of a purely administrative nature involving no change to the properties or efficacy of the biocidal product or biocidal product family;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/ab/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/ab" id="article-3-1-ab">
<Pnumber PuncBefore="(" PuncAfter=")">ab</Pnumber>
<P3para>
<Text>‘minor change’ means an amendment of an existing authorisation that is not of a purely administrative nature and requires only a limited re-assessment of the properties or efficacy of the biocidal product or biocidal product family;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/ac/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/ac" id="article-3-1-ac">
<Pnumber PuncBefore="(" PuncAfter=")">ac</Pnumber>
<P3para>
<Text>‘major change’ means an amendment of an existing authorisation which is neither an administrative change nor a minor change;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/ad/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/ad" id="article-3-1-ad">
<Pnumber PuncBefore="(" PuncAfter=")">ad</Pnumber>
<P3para>
<Text>‘vulnerable groups’ means persons needing specific consideration when assessing the acute and chronic health effects of biocidal products. These include pregnant and nursing women, the unborn, infants and children, the elderly and, when subject to high exposure to biocidal products over the long term, workers and residents;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/ae/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/ae" id="article-3-1-ae">
<Pnumber PuncBefore="(" PuncAfter=")">ae</Pnumber>
<P3para>
<Text>
‘small and medium-sized enterprises’ or ‘SMEs’ means small and medium-sized enterprises as defined in Commission Recommendation 2003/361/EC of 6 May 2003 concerning the definition of micro, small and medium-sized enterprises
<FootnoteRef Ref="f00040"/>
.
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/af/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/af" id="article-3-1-af">
<Pnumber PuncBefore="(" PuncAfter=")">
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">af</Addition>
</Pnumber>
<P3para>
<Text>
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">‘the consent requirement’ means the requirement for consent in accordance with Article 83B;</Addition>
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/ag/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/ag" id="article-3-1-ag">
<Pnumber PuncBefore="(" PuncAfter=")">
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">ag</Addition>
</Pnumber>
<P3para>
<Text>
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">‘the UK List’ means the list of approved substances established and maintained in accordance with Article 8A;</Addition>
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/ah/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/ah" id="article-3-1-ah">
<Pnumber PuncBefore="(" PuncAfter=")">
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">ah</Addition>
</Pnumber>
<P3para>
<Text>
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">‘the Simplified Active Substance List’ means the list of active substances which can be used in biocidal products that qualify for the simplified authorisation procedure, established and maintained in accordance with Article 24A.</Addition>
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/ai/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/ai" id="article-3-1-ai">
<Pnumber PuncBefore="(" PuncAfter=")">
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">ai</Addition>
</Pnumber>
<P3para>
<Text>
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">“appropriate fee” means the fee payable for the activity concerned in regulations made under section 43 of the Health and Safety at Work etc. Act 1974 where the competent authority is appointed in accordance with regulation 5 of the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013;</Addition>
</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/aj/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/aj" id="article-3-1-aj">
<Pnumber PuncBefore="(" PuncAfter=")">
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">aj</Addition>
</Pnumber>
<P3para>
<Text>
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">“Devolved Authority” means—</Addition>
</Text>
<P4 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/aj/i/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/aj/i" id="article-3-1-aj-i">
<Pnumber PuncBefore="(" PuncAfter=")">
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">i</Addition>
</Pnumber>
<P4para>
<Text>
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">the Scottish Ministers, or</Addition>
</Text>
</P4para>
</P4>
<P4 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/1/aj/ii/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/aj/ii" id="article-3-1-aj-ii">
<Pnumber PuncBefore="(" PuncAfter=")">
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">ii</Addition>
</Pnumber>
<P4para>
<Text>
<Addition ChangeId="key-83f2de1fa2d210de4ec8ad052195f5d8-1722007167001" CommentaryRef="key-83f2de1fa2d210de4ec8ad052195f5d8">the Welsh Ministers.</Addition>
</Text>
</P4para>
</P4>
</P3para>
</P3>
</P2para>
</P2>
<P2 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/2/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/2" id="article-3-2">
<Pnumber PuncBefore="" PuncAfter=".">2</Pnumber>
<P2para>
<Text>For the purposes of this Regulation, the definitions laid down in Article 3 of Regulation (EC) No 1907/2006 shall apply for the following terms:</Text>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/2/a/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/2/a" id="article-3-2-a">
<Pnumber PuncBefore="(" PuncAfter=")">a</Pnumber>
<P3para>
<Text>‘substance’;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/2/b/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/2/b" id="article-3-2-b">
<Pnumber PuncBefore="(" PuncAfter=")">b</Pnumber>
<P3para>
<Text>‘mixture’;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/2/c/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/2/c" id="article-3-2-c">
<Pnumber PuncBefore="(" PuncAfter=")">c</Pnumber>
<P3para>
<Text>‘article’;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/2/d/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/2/d" id="article-3-2-d">
<Pnumber PuncBefore="(" PuncAfter=")">d</Pnumber>
<P3para>
<Text>‘product and process-orientated research and development’;</Text>
</P3para>
</P3>
<P3 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/2/e/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/2/e" id="article-3-2-e">
<Pnumber PuncBefore="(" PuncAfter=")">e</Pnumber>
<P3para>
<Text>‘scientific research and development’.</Text>
</P3para>
</P3>
</P2para>
</P2>
<P2 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/3/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/3" id="article-3-3">
<Pnumber PuncBefore="" PuncAfter=".">
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">3</Substitution>
</Pnumber>
<P2para>
<Text>
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">The Secretary of State may issue a decision which is to be published, as to whether a substance is a nanomaterial, having regard in particular to Commission Recommendation 2011/696/EU of 18 October 2011 on the definition of nanomaterial and whether a specific product or group of products is a biocidal product or a treated article or neither.</Substitution>
</Text>
</P2para>
</P2>
<P2 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/4/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/4" id="article-3-4">
<Pnumber PuncBefore="" PuncAfter=".">
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">4</Substitution>
</Pnumber>
<P2para>
<Text>
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">A decision issued under paragraph 3 above is subject to the consent requirement.</Substitution>
</Text>
</P2para>
</P2>
<P2 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/5/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/5" id="article-3-5">
<Pnumber PuncAfter=".">
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">5</Substitution>
</Pnumber>
<P2para>
<Text>
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">The Secretary of State may by regulations adapt the definition of nanomaterial set out in point (z) of paragraph 1 of this Article in view of technical and scientific progress, taking into account the Recommendation referred to in paragraph 3 above.</Substitution>
</Text>
</P2para>
</P2>
<P2 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/6/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/6" id="article-3-6">
<Pnumber PuncAfter=".">
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">6</Substitution>
</Pnumber>
<P2para>
<Text>
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">Regulations made under paragraph 5 above are subject to the consent requirement.</Substitution>
</Text>
</P2para>
</P2>
<P2 DocumentURI="http://www.legislation.gov.uk/eur/2012/528/article/3/7/2020-12-31" IdURI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/7" id="article-3-7">
<Pnumber PuncAfter=".">
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">7</Substitution>
</Pnumber>
<P2para>
<Text>
<Substitution ChangeId="key-3568e92e35da19a0f4735fd4bace5d6b-1722007167000" CommentaryRef="key-3568e92e35da19a0f4735fd4bace5d6b">Where any of the Devolved Authorities makes proposals in relation to adaptations under paragraph 5 above, the Secretary of State must have regard to such proposals in deciding whether to exercise functions in that paragraph.</Substitution>
</Text>
</P2para>
</P2>
</P1para>
</P1>
</P1group>
</EUChapter>
</EUBody>
</EURetained>
<Footnotes>
<Footnote id="f00040">
<FootnoteText>
<Para>
<Text>
<Citation id="c00042" Class="EuropeanUnionOfficialJournal" Year="2003" URI="https://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv:OJ.L_.2003.124.01.0036.01.ENG" Date="2003-05-20">OJ L 124, 20.5.2003, p. 36</Citation>
.
</Text>
</Para>
</FootnoteText>
</Footnote>
</Footnotes>
<Commentaries>
<Commentary Type="F" Source="EU" id="c000001">
<Para>
<Text>
Substituted by
<Citation URI="http://www.legislation.gov.uk/id/eur/2014/334" id="ccd13e7884202407251245045390100" Class="EuropeanUnionRegulation" Year="2014" Number="334" Title="Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market (Text with EEA relevance)">Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market (Text with EEA relevance)</Citation>
.
</Text>
</Para>
</Commentary>
<Commentary Type="F" Source="EU" id="c000002">
<Para>
<Text>
Deleted by
<Citation URI="http://www.legislation.gov.uk/id/eur/2014/334" id="ccd13e7891202407251245045390100" Class="EuropeanUnionRegulation" Year="2014" Number="334" Title="Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market (Text with EEA relevance)">Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market (Text with EEA relevance)</Citation>
.
</Text>
</Para>
</Commentary>
<Commentary id="key-3568e92e35da19a0f4735fd4bace5d6b" Type="F">
<Para>
<Text>
<CitationSubRef id="cgp5qkm95-00006" StartSectionRef="article-3-3" EndSectionRef="article-3-7" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/3" UpTo="http://www.legislation.gov.uk/id/eur/2012/528/article/3/7">Art. 3(3)-(7)</CitationSubRef>
substituted for
<CitationSubRef id="cgp5qkm95-00007" SectionRef="article-3-3" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/3">Art. 3(3)</CitationSubRef>
(31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00008" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00008" id="cgp5qkm95-00009" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00008" id="cgp5qkm95-00010" SectionRef="schedule-2-paragraph-64-3" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/3" Operative="true">Sch. 2 para. 64(3)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00011" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00011" id="cgp5qkm95-00012" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-83f2de1fa2d210de4ec8ad052195f5d8" Type="F">
<Para>
<Text>
<CitationSubRef id="ccd8e1202407261634540810100" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/af" UpTo="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/aj" Type="group" StartSectionRef="article-3-1-af" EndSectionRef="article-3-1-aj">Art. 3(1)(af)-(aj)</CitationSubRef>
inserted (31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="d10e4" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="d10e4" id="ccd8e7202407261634540810100" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2" SectionRef="regulation-1-2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="d10e4" id="ccd8e10202407261634540810100" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/k" Operative="true" SectionRef="schedule-2-paragraph-64-2-k">Sch. 2 para. 64(2)(k)</CitationSubRef>
(as amended by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2020/1567" id="d10e13" Class="UnitedKingdomStatutoryInstrument" Year="2020" Number="1567">S.I. 2020/1567</Citation>
,
<CitationSubRef CitationRef="d10e13" id="ccd8e16202407261634540810100" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/regulation/1/2" SectionRef="regulation-1-2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="d10e13" id="ccd8e20202407261634540810100" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/schedule/2/paragraph/23/d" Operative="true" SectionRef="schedule-2-paragraph-23-d">Sch. 2 para. 23(d)</CitationSubRef>
);
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="d10e23" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="d10e23" id="ccd8e26202407261634540810100" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1" Operative="true" SectionRef="schedule-5-paragraph-1-1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-079279b6dc84aef1ddedc2aef184bc04" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00029" SectionRef="article-3-1-d" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/d">Art. 3(1)(d)</CitationSubRef>
inserted (31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00030" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00030" id="cgp5qkm95-00031" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00030" id="cgp5qkm95-00032" SectionRef="schedule-2-paragraph-64-2-a" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/a" Operative="true">Sch. 2 para. 64(2)(a)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00033" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00033" id="cgp5qkm95-00034" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-9aae6502fa09e9593f160e229e195dd7" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00040" SectionRef="article-3-1-e" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/e">Art. 3(1)(e)</CitationSubRef>
inserted (31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00041" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00041" id="cgp5qkm95-00042" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00041" id="cgp5qkm95-00043" SectionRef="schedule-2-paragraph-64-2-b" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/b" Operative="true">Sch. 2 para. 64(2)(b)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00044" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00044" id="cgp5qkm95-00045" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-041aa773d22be02ee7d09c8025e339d5" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00062" SectionRef="article-3-1-k" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/k">Art. 3(1)(k)</CitationSubRef>
substituted (31.12.2020) by S.I. 2019/720, Sch. 2 para. 64(2)(d) (as substituted by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2020/1567" id="cgp5qkm95-00063" Class="UnitedKingdomStatutoryInstrument" Year="2020" Number="1567" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00063" id="cgp5qkm95-00064" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00063" id="cgp5qkm95-00065" SectionRef="schedule-2-paragraph-23-a" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/schedule/2/paragraph/23/a" Operative="true">Sch. 2 para. 23(a)</CitationSubRef>
)
</Text>
</Para>
</Commentary>
<Commentary id="key-0c94da28836a7d27a4a884df261fd5c2" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00071" SectionRef="article-3-1-m" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/m">Art. 3(1)(m)</CitationSubRef>
omitted (31.12.2020) by virtue of
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00072" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00072" id="cgp5qkm95-00073" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00072" id="cgp5qkm95-00074" SectionRef="schedule-2-paragraph-64-2-e-i" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/e/i" Operative="true">Sch. 2 para. 64(2)(e)(i)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00075" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00075" id="cgp5qkm95-00076" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-02fdc78c2e488e126ad2ea45edeb1a4d" Type="F">
<Para>
<Text>
<CitationSubRef id="ccd8e1202407261629537140100" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/n" SectionRef="article-3-1-n">Art. 3(1)(n)</CitationSubRef>
substituted (31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="d10e4" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="d10e4" id="ccd8e7202407261629537140100" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2" SectionRef="regulation-1-2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="d10e4" id="ccd8e10202407261629537140100" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/f" Operative="true" SectionRef="schedule-2-paragraph-64-2-f">Sch. 2 para. 64(2)(f)</CitationSubRef>
(as amended by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2020/1567" id="d10e13" Class="UnitedKingdomStatutoryInstrument" Year="2020" Number="1567">S.I. 2020/1567</Citation>
,
<CitationSubRef CitationRef="d10e13" id="ccd8e16202407261629537140100" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/regulation/1/2" SectionRef="regulation-1-2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="d10e13" id="ccd8e20202407261629537140100" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/schedule/2/paragraph/23/b" Operative="true" SectionRef="schedule-2-paragraph-23-b">Sch. 2 para. 23(b)</CitationSubRef>
);
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="d10e23" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="d10e23" id="ccd8e26202407261629537140100" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1" Operative="true" SectionRef="schedule-5-paragraph-1-1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-6f779ceee8ef57ddc03710443bf4e989" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00114" SectionRef="article-3-1-o" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/o">Art. 3(1)(o)</CitationSubRef>
omitted (31.12.2020) by virtue of
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00115" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00115" id="cgp5qkm95-00116" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00115" id="cgp5qkm95-00117" SectionRef="schedule-2-paragraph-64-2-g" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/g" Operative="true">Sch. 2 para. 64(2)(g)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00118" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00118" id="cgp5qkm95-00119" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-76fa6c0e1db399c99946e73f876511d2" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00134" SectionRef="article-3-1-p" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/p">Art. 3(1)(p)</CitationSubRef>
substituted (31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00135" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00135" id="cgp5qkm95-00136" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00135" id="cgp5qkm95-00137" SectionRef="schedule-2-paragraph-64-2-h-i" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/h/i" Operative="true">Sch. 2 para. 64(2)(h)(i)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00138" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00138" id="cgp5qkm95-00139" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-67d8c02b194f8fb2047f182a9c8d0b73" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="ccd8e2202407261631069990100" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/p" SectionRef="article-3-1-p">Art. 3(1)(p)</CitationSubRef>
substituted (31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="d10e5" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="d10e5" id="ccd8e8202407261631069990100" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2" SectionRef="regulation-1-2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="d10e5" id="ccd8e11202407261631069990100" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/h/ii" Operative="true" SectionRef="schedule-2-paragraph-64-2-h-ii">Sch. 2 para. 64(2)(h)(ii)</CitationSubRef>
(as amended by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2020/1567" id="d10e14" Class="UnitedKingdomStatutoryInstrument" Year="2020" Number="1567">S.I. 2020/1567</Citation>
,
<CitationSubRef CitationRef="d10e14" id="ccd8e18202407261631069990100" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/regulation/1/2" SectionRef="regulation-1-2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="d10e14" id="ccd8e21202407261631069990100" URI="http://www.legislation.gov.uk/id/uksi/2020/1567/schedule/2/paragraph/23/c" Operative="true" SectionRef="schedule-2-paragraph-23-c">Sch. 2 para. 23(c)</CitationSubRef>
);
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="d10e24" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="d10e24" id="ccd8e27202407261631069990100" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1" Operative="true" SectionRef="schedule-5-paragraph-1-1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-c36c9df52a8d7f2e197162dc5bb09929" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00156" SectionRef="article-3-1-t" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/t">Art. 3(1)(t)</CitationSubRef>
inserted (31.12.2020) by
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00157" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00157" id="cgp5qkm95-00158" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00157" id="cgp5qkm95-00159" SectionRef="schedule-2-paragraph-64-2-i" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/i" Operative="true">Sch. 2 para. 64(2)(i)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00160" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00160" id="cgp5qkm95-00161" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-0045341a450f3705c91f61b32137f157" Type="F">
<Para>
<Text>
<CitationSubRef id="cgp5qkm95-00165" SectionRef="article-3-1-x" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/x">Art. 3(1)(x)</CitationSubRef>
omitted (31.12.2020) by virtue of
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00166" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00166" id="cgp5qkm95-00167" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00166" id="cgp5qkm95-00168" SectionRef="schedule-2-paragraph-64-2-j" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/j" Operative="true">Sch. 2 para. 64(2)(j)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00169" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00169" id="cgp5qkm95-00170" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-8d323ec30d9173ae28717d545691e89c" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00082" SectionRef="article-3-1-m" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/m">Art. 3(1)(m)</CitationSubRef>
omitted (31.12.2020) by virtue of
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00083" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00083" id="cgp5qkm95-00084" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00083" id="cgp5qkm95-00085" SectionRef="schedule-2-paragraph-64-2-e-ii" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/e/ii" Operative="true">Sch. 2 para. 64(2)(e)(ii)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00086" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00086" id="cgp5qkm95-00087" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
</Text>
</Para>
</Commentary>
<Commentary id="key-d2c824c8bb655b17dae9ea8f98e36cbb" Type="F">
<Para>
<Text>
Words in
<CitationSubRef id="cgp5qkm95-00051" SectionRef="article-3-1-f" URI="http://www.legislation.gov.uk/id/eur/2012/528/article/3/1/f">Art. 3(1)(f)</CitationSubRef>
omitted (31.12.2020) by virtue of
<Citation URI="http://www.legislation.gov.uk/id/uksi/2019/720" id="cgp5qkm95-00052" Class="UnitedKingdomStatutoryInstrument" Year="2019" Number="720" Title="The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019">The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720)</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00052" id="cgp5qkm95-00053" SectionRef="regulation-1-2" URI="http://www.legislation.gov.uk/id/uksi/2019/720/regulation/1/2">reg. 1(2)</CitationSubRef>
,
<CitationSubRef CitationRef="cgp5qkm95-00052" id="cgp5qkm95-00054" SectionRef="schedule-2-paragraph-64-2-c" URI="http://www.legislation.gov.uk/id/uksi/2019/720/schedule/2/paragraph/64/2/c" Operative="true">Sch. 2 para. 64(2)(c)</CitationSubRef>
;
<Citation URI="http://www.legislation.gov.uk/id/ukpga/2020/1" id="cgp5qkm95-00055" Year="2020" Class="UnitedKingdomPublicGeneralAct" Number="1">2020 c. 1</Citation>
,
<CitationSubRef CitationRef="cgp5qkm95-00055" id="cgp5qkm95-00056" SectionRef="schedule-5-paragraph-1-1" URI="http://www.legislation.gov.uk/id/ukpga/2020/1/schedule/5/paragraph/1/1">Sch. 5 para. 1(1)</CitationSubRef>
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