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

S.I. 2019/273 · Made 8 February 2019 · Extends to Northern Ireland

Up to date with all changes known to legislation.gov.uk, revised to 31 December 2020.

Exiting The European Union, Northern Ireland

Animals, Northern Ireland

Sift requirements satisfied 31st January 2019

Made 8th February 2019

Laid before Parliament 18th 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(b) of Schedule 7 to, the European Union (Withdrawal) Act 2018 M1.

The requirements of paragraph 3(2) of Schedule 7 of the European Union (Withdrawal) Act 2018 (relating to the appropriate Parliamentary procedure for these Regulations) have been satisfied.

Annotations to the whole text

Marginal citations

M1

2018 c.16

Contents

  1. 1Citation, commencement and extent
  2. 2Amendment to the Mechanically Recovered Meat (Export Prohibition) Order (Northern Ireland) 1995
  3. 3Amendment to the Animal By-Products (Enforcement) Regulations (Northern Ireland) 2015 Not yet in force
  4. 4Amendment to the Transmissible Spongiform Encephalopathies Regulations (Northern Ireland) 2018
  5. Signature
  6. Explanatory note

1Citation, commencement and extentI1

(1)

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

(2)

These Regulations extend to Northern Ireland only.

2Amendment to the Mechanically Recovered Meat (Export Prohibition) Order (Northern Ireland) 1995I1

In Article 3 of the Mechanically Recovered Meat (Export Prohibition) Order (Northern Ireland) 1995 M1, for “another” substitute “ a ”.

3Amendment to the Animal By-Products (Enforcement) Regulations (Northern Ireland) 2015F1

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

4Amendment to the Transmissible Spongiform Encephalopathies Regulations (Northern Ireland) 2018I1

(1)

The Transmissible Spongiform Encephalopathies Regulations (Northern Ireland) 2018 M1 are amended as follows.

F1(2)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(3)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(4)

In Schedule 2, for paragraph 11(2) substitute—

“(2)

In this Schedule an “approved testing laboratory” means—

(a)

a laboratory approved by the Department under this paragraph; or

(b)

a laboratory approved under corresponding legislation elsewhere in the United Kingdom.”

F2(5)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(6)

In Schedule 7—

(a)

in paragraph 1, omit “placed on the member State”;

F3(b)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(c)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(d)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F4(7)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Signature

Gardiner of Kimble

Parliamentary Under Secretary of State

Department for Environment, Food and Rural Affairs

Explanatory note

(This note is not part of the Regulations)

These Regulations are made in exercise of the powers conferred by section 8(1) of the European Union (Withdrawal) Act 2018 (c.16) in order to address the failures of retained EU legislation to operate effectively and other deficiencies (in particular paragraphs (a), (d) and (g) of section 8(2)) arising from the withdrawal of the United Kingdom from the European Union.

These Regulations amend domestic legislation applying to Northern Ireland that provides enforcement of—

  1. (a)

    the Transmissible Spongiform Encephalopathies Regulation (EC) No 999/2001 laying down rules for the prevention, control and eradication of certain transmissible spongiform encephalopathies;

  2. (b)

    the Animal By-Products Regulation (EC) No 1069/2009 laying down health rules as regards animal by-products and derived products not intended for human consumption; and

  3. (c)

    Commission Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009.

An impact assessment has not been produced for this instrument as no, or no significant, impact on private, voluntary or public sector is foreseen.