- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/07/2017)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Regulation (EC) No 999/2001 of the European Parliament and of the Council of 22 May 2001 laying down rules for the prevention, control and eradication of certain transmissible spongiform encephalopathies
When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.
Mae unrhyw newidiadau sydd wedi cael eu gwneud yn barod gan y tîm yn ymddangos yn y cynnwys a chyfeirir atynt gydag anodiadau.Ar ôl y diwrnod ymadael bydd tair fersiwn o’r ddeddfwriaeth yma i’w gwirio at ddibenion gwahanol. Y fersiwn legislation.gov.uk yw’r fersiwn sy’n weithredol yn y Deyrnas Unedig. Y Fersiwn UE sydd ar EUR-lex ar hyn o bryd yw’r fersiwn sy’n weithredol yn yr UE h.y. efallai y bydd arnoch angen y fersiwn hon os byddwch yn gweithredu busnes yn yr UE. EUR-Lex Y fersiwn yn yr archif ar y we yw’r fersiwn swyddogol o’r ddeddfwriaeth fel yr oedd ar y diwrnod ymadael cyn cael ei chyhoeddi ar legislation.gov.uk ac unrhyw newidiadau ac effeithiau a weithredwyd yn y Deyrnas Unedig wedyn. Mae’r archif ar y we hefyd yn cynnwys cyfraith achos a ffurfiau mewn ieithoedd eraill o EUR-Lex. The EU Exit Web Archive legislation_originated_from_EU_p3
There are currently no known outstanding effects for the Regulation (EC) No 999/2001 of the European Parliament and of the Council.
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
CHAPTER VI REFERENCE LABORATORIES, SAMPLING, TESTING AND CONTROLS
I. MONITORING IN BOVINE ANIMALS
3. Monitoring in animals not slaughtered for human consumption
4. Monitoring in animals purchased for destruction pursuant to Regulation (EC)...
7. Revision of the annual monitoring programmes concerning BSE (BSE monitoring...
CHAPTER B REPORTING AND RECORDING REQUIREMENTS
I. REQUIREMENTS ON MEMBER STATES
A. Information to be presented by Member States in their annual...
1. The number of suspected cases placed under official movement restrictions...
2. The number of suspected cases subject to laboratory examination in...
3. The number of flocks where suspected cases in ovine and...
4. The number of bovine animals tested within each subpopulation referred...
5. The number of ovine and caprine animals and flocks tested...
6. The geographical distribution, including the country of origin if not...
7. In animals other than bovine, ovine and caprine animals, the...
8. The genotype, and, where possible, the breed, of each ovine...
CHAPTER I Extensions of the prohibition provided for in Article 7(1)
CHAPTER II Derogations from the prohibitions provided for in Article 7(1) and...
CHAPTER III General conditions for the application of certain derogations provided for...
CHAPTER IV Specific conditions for the application of derogations provided for in...
SECTION A Specific conditions applicable to the production and the use of...
SECTION B Specific conditions applicable to the use of dicalcium phosphate and...
SECTION C Specific conditions applicable to the production and use of blood...
SECTION D Specific conditions applicable to the production and use of processed...
SECTION E Specific conditions applicable to the production, placing on the market...
SECTION F Specific conditions applicable to the production and use of processed...
CHAPTER V General requirements
SECTION B Transport of feed materials and compound feed containing products derived...
SECTION C Production of compound feed containing products derived from ruminants
SECTION D Use and storage on farms of feed materials and compound...
SECTION E Export of processed animal protein and products containing such protein...
CONTROL AND ERADICATION OF TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES
CHAPTER A Measures following the suspicion of the presence of a TSE...
CHAPTER B Measures following confirmation of the presence of a TSE in...
CHAPTER C Minimum requirements for a breeding programme for resistance to TSEs...
1. The breeding programme shall concentrate on flocks of high genetic...
2. A database shall be established containing at least the following...
3. A system of uniform certification shall be established in which...
4. A system for the identification of animals and samples, the...
5. Genotyping of blood or other tissues collected for the purposes...
6. The competent authority of the Member State may assist breed...
7. Breeding programmes shall be drawn up for each breed, taking...
PART 3 Specific rules for breeding rams sampled in flocks not participating...
PART 4 The framework for the recognition of the TSE-resistant status of...
PART 5 Reports to be provided to the Commission by the Member...
PLACING ON THE MARKET AND EXPORT
CHAPTER A Conditions for intra-Union trade in live animals, semen and embryos
CHAPTER C Conditions for intra-Community trade in certain products of animal origin
IMPORTATION INTO THE UNION OF LIVE ANIMALS, EMBRYOS, OVA AND PRODUCTS OF ANIMAL ORIGIN
CHAPTER C Imports of products of animal origin from bovine, ovine or...
SECTION B Imports from a country or a region with a negligible...
SECTION C Imports from a country or a region with a controlled...
1. Imports of products of bovine, ovine and caprine animal origin...
2. For products of bovine animal origin, by way of derogation...
3. When the removal of the vertebral column is required, carcasses...
4. The number of bovine carcasses or wholesale cuts of carcasses,...
5. In the case of intestines originally sourced from a country...
SECTION D Imports from a country or a region with an undetermined...
1. Imports of products of bovine, ovine and caprine animal origin...
2. For products of bovine animal origin, by way of derogation...
3. When removal of the vertebral column is required, carcasses or...
4. Specific information on the number of bovine carcasses or wholesale...
5. In the case of intestines originally sourced from a country...
CHAPTER D Imports of animal by-products and derived products from bovine, ovine...
CHAPTER F Imports of products of animal origin from farmed and wild...
REFERENCE LABORATORIES, SAMPLING AND LABORATORY ANALYSIS METHODS
The Whole Regulation you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Y Rhestrau you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE): Mae'r wreiddiol version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.
Pwynt Penodol mewn Amser: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search.
Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:
Mae’r llinell amser yma yn dangos y fersiynau gwahanol a gymerwyd o EUR-Lex yn ogystal ag unrhyw fersiynau dilynol a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig.
Cymerir dyddiadau fersiynau’r UE o ddyddiadau’r dogfennau ar EUR-Lex ac efallai na fyddant yn cyfateb â’r adeg pan ddaeth y newidiadau i rym ar gyfer y ddogfen.
Ar gyfer unrhyw fersiynau a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig, bydd y dyddiad yn cyd-fynd â’r dyddiad cynharaf y daeth y newid (e.e. ychwanegiad, diddymiad neu gyfnewidiad) a weithredwyd i rym. Am ragor o wybodaeth gweler ein canllaw i ddeddfwriaeth ddiwygiedig ar Ddeall Deddfwriaeth.
Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:
liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys