The Transmissible Spongiform Encephalopathies and Animal By-Products (Amendment etc.) (EU Exit) Regulations 2019

Type Statutory-Instrument
Publication 2019-01-31
State In force
Department King's Printer of Acts of Parliament
Reform history JSON API PDF

Made: 31st January 2019

Laid before Parliament: 4th February 2019

Coming into force in accordance with regulation 1

The Secretary of State makes these Regulations in exercise of the powers conferred by section 8(1) of, and paragraph 21 of Schedule 7 to, the European Union (Withdrawal) Act 2018 .

The requirements of paragraph 3(2) of Schedule 7 to the Act (relating to the appropriate Parliamentary procedure for these Regulations) have been satisfied.

Citation and commencement

1

These Regulations may be cited as the Transmissible Spongiform Encephalopathies and Animal By-Products (Amendment etc.) (EU Exit) Regulations 2019 and come into force on exit day.

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

2

(q) constituent nation: one of the following nations of the British Islands: England, Guernsey, Isle of Man, Jersey, Scotland or Wales; (r) OIE: the World Organisation for Animal Health.

(1A) In this Regulation, “appropriate authority” means: (a) in relation to England, the Secretary of State; (b) in relation to Wales, the Welsh Ministers; (c) in relation to Scotland, theScottish Ministers; (d) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . (1B) But the appropriate authority is the Secretary of State if consent is given by: (a) in relation to Wales, the Welsh Ministers; (b) relation to Scotland, the Scottish Ministers; (c) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(1) The BSE status of countries and regions as categorised by the OIE is— (a) negligible risk, (b) controlled risk, or (c) undetermined risk, and, as at exit day, the BSE status for each of the constituent nations is established by Commission Decision 2007/453.

(6) Exporting countries that are eligible for inclusion in the list of countries or regions approved for the import into Great Britain of live animals or of the products covered by this Regulation must be categorised with regard to BSE status that takes into account the criteria and potential risk factors set out in paragraph 1, and any statistical survey of the epidemiological situation regarding TSEs in the country on the basis of the use, in a screening procedure, of rapid tests. The classification criteria used by the OIE must be taken into account. Eligibility to import from a third country into Great Britain live animals or products of animal origin within scope of this Regulation under conditions determined on their established category must be established as soon as possible, once any epidemiological or other evidence which might lead to a change in BSE status has been analysed by the appropriate authorities.

(1) Specified risk material, referred to and listed in Annex 5 and including at least the brain, spinal cord, eyes and tonsils of bovine animals aged over 12 months, and the vertebral column of bovine animals aged over 30 months, must— (a) be removed and disposed of in accordance with Annex 5 and with Regulation (EC) No 1069/2009; (b) not be imported into Great Britain from any country other than a member State. (2) Tissues from animals which have undergone one of the alternative tests listed in Annex 10, which is applied under the conditions provided for in Annex 5, and in relation to which the test results are negative, are not to be regarded as specified risk material.

Any person who suspects an animal of being infected by a TSE must immediately notify the relevant competent authority.

Appropriate health certificates relating to trade in the semen, embryos and ova of bovine, ovine or caprine animals, and appropriate commercial documents relating to trade in products of animal origin must be supplemented, where necessary, by a reference to the category specifying the BSE classification.

The appropriate health certificates relating to imports must be supplemented in respect of the BSE classification of any country by the specific requirements laid down in Annex 9, as soon as that classification is confirmed.

The appropriate authority may carry out monitoring for TSEs in cervids.

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