Skip to content
Nelum
Laws of United Kingdom

Export Restrictions (Foot-and-Mouth Disease) (Amendment No. 3) Regulations (Northern Ireland) 2007 (S.R. No. 441 of 2007)

Made 2007-10-23 · Text as of 2026-10-01

Public law and official guidance, published as research. Not legal, tax or financial advice.

About this law

Language
English
Kind
Regulation
Country
United Kingdom · Northern Ireland
Subjects
Livestock, Food and nutrition
Keywords
animal health, international trade, pests/diseases, food safety and quality, meat, milk/dairy products
Categories
*

Where to read it

    No source link is recorded for this law.

Text

The law's own text, section by section, as held. Each section has its own link.

  1. S T A T U T O R Y R U L E S O F N O R T H E R N I R E L A N D 2007 No. 441 ANIMALS ANIMAL HEALTH The Export Restrictions (Foot-and-Mouth Disease) (Amendment No. 3) Regulations (Northern Ireland) 2007 Made - - - - 23rd October 2007 Coming into operation - 24th October 2007 The Department of Agriculture and Rural Development, is designated(a) for the purposes of section 2(2) of the European Communities Act 1972(b), in relation to the common agricultural policy of the European Community. The Department of Agriculture and Rural Development makes the following Regulations in exercise of the powers conferred upon it by section 2(2) of the European Communities Act 1972. Citation and commencement 1. These Regulations may be cited as The Export Restrictions (Foot-and-Mouth Disease) (Amendment No. 3) Regulations (Northern Ireland) 2007 and come into operation on 24th October 2007. Interpretation 2. The Interpretation Act (Northern Ireland) 1954(c) shall apply to these Regulations as it applies to an Act of the Northern Ireland Assembly. Amendment 3.—(1) The Export Restrictions (Foot-and-Mouth Disease) Regulations (Northern Ireland) 2007(d) are amended as follows. (2) In regulation 2 (Interpretation) for the definition of “the Decision” substitute— ““the Decision” means Commission Decision 2007/554/EC concerning certain protection measures against foot-and-mouth disease in the United Kingdom(e) as amended by Commission Decision 2007/588/EC(f), Commission Decision (a) S.I. 2000/2812 (b) 1972 c. 68 (c) 1954 c. 33 (N.I.) (d) S.R. 2007 No. 357 as amended by S.R. 2007 No. 364 and S.R. 2007 No. 399 (e) O.J. No. L210, 10.8.2007, p. 36 (f) O.J. No. L220, 25.8.2007, p. 27 2 2007/608/EC(a), Commission Decision 2007/663/EC(b) and Commission Decision 2007/664/EC(c);”. (3) In regulation 8 (Dispatch of semen, ova and embryos) after (c) insert— “(d) the health certificate accompanying ovine or caprine semen shall bear the following words— “Frozen ovine/caprine semen conforming to Commission Decision 2007/554/EC of 9 August 2007 concerning certain protection measures against foot-and-mouth disease in the United Kingdom.”. (e) The health certificate accompanying ovine or caprine embryos shall bear the following words— “Frozen ovine/caprine embryos conforming to Commission Decision 2007/554/EC of 9 August 2007 concerning certain protection measures against foot-and-mouth disease in the United Kingdom.””. (4) In regulation 10 (Dispatch of animal products) for paragraph 7(b) substitute— “(b) medicinal products as defined in Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community Code relating to medicinal products for human use(d), medical devices manufactured utilising animal tissue which is rendered non-viable as referred to in Article 1(5)(g) of Directive 93/42/EEC, veterinary medicinal products as defined in Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community Code relating to veterinary medicinal products(e) and investigational medicinal products as defined in Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the conduct of clinical trials on medicinal products for human use(f), provided they are accompanied by a commercial document stating that the products are for use as in-vitro diagnostic, laboratory reagents, medical products or medical devices and the products are clearly labelled “for in-vitro diagnostic use only” or “for laboratory use only” as “medicinal products” or as “medical devices”.”. Sealed with the Official Seal of the Department of Agriculture and Rural Development on 23rd October 2007. Elizabeth Redmond A senior officer of the Department of Agriculture and Rural Development (a) O.J. No. L241, 14.9.2007, p. 26 (b) O.J. No. L270, 13.10.2007, p. 18 (c) O.J. No. L370, 13.10.2007, p. 21 (d) O.J. No. L311, 28.11.2001, p. 67 (e) O.J. No. L311, 28.11.2001, p. 1 (f) O.J. No. L121, 1.5.2001, p. 34 3 EXPLANATORY NOTE (This note is not part of the Regulations) These Regulations amend The Export Restrictions (Foot-and-Mouth Disease) Regulations (Northern Ireland) 2007 (S.R. 2007 No. 357 as amended by S.R. 2007 No. 364 and S.R. 2007 No. 399). The Regulations give effect to Commission Decision 2007/663/EC of 12th October 2007 and Commission Decision 2007/664/EC of 12th October 2007 which amend Commission Decision 2007/554/EC concerning certain protection measures against foot-and-mouth disease in the United Kingdom. Published and printed in the UK by The Stationery Office Limited under the authority and superintendence of Carol Tullo, Controller of Her Majesty’s Stationery Office being the Government Printer for Northern Ireland and the Officer appointed to print the Acts of the Northern Ireland Assembly Dd. N3410. C2. 10/07. Gp. 130. 14567.

Export Restrictions (Foot-and-Mouth Disease) (Amendment No. 3) Regulations (Northern Ireland) 2007 (S.R. No. 441 of 2007) · Nelum