The Animal Health and Welfare and Official Controls (Agriculture) (EU Exit) (Scotland) (Amendment) Regulations 2020
PART 1INTRODUCTION
Citation and commencement1.
(1)
These Regulations may be cited as the Animal Health and Welfare and Official Controls (Agriculture) (EU Exit) (Scotland) (Amendment) Regulations 2020.
(2)
These Regulations, except for regulation 4, come into force immediately before IP completion day.
(3)
Regulation 4 comes into force on IP completion day.
PART 2AMENDMENT OF SECONDARY LEGISLATION IN EXERCISE OF POWERS UNDER SECTION 2(2) OF THE EUROPEAN COMMUNITIES ACT 1972
Amendment of the Welfare of Animals at the Time of Killing (Scotland) Regulations 20122.
“(i)
recognised and regulated by the Scottish Qualifications Authority5 or an equivalent body in England, Wales or Northern Ireland; and”.
PART 3AMENDMENT OF SECONDARY LEGISLATION TO ADDRESS DEFICIENCIES ARISING FROM THE WITHDRAWAL OF THE UNITED KINGDOM FROM THE EUROPEAN UNION
Amendment of the Animal Health (EU Exit) (Scotland) (Amendment) Regulations 20193.
(1)
(2)
“(ia)
in sub-paragraph (1), in the opening words, for “another” substitute “a”;”.
(3)
In regulation 22 (amendment of the Bovine Semen (Scotland) Regulations 2007)—
(a)
in paragraph (6)(b)—
(i)
“(bb)
in relation to another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(ii)
“(bb)
in relation to another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(b)
in paragraph (11)—
(i)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(ii)
in sub-paragraph (b)—
(aa)
“(ii)
in relation to another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(bb)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to;”,
(cc)
“(b)
the references to “certification” include a “certificate” as defined in these Regulations or an equivalent certificate published by an authority in another part of the United Kingdom under legislation in force there;”,
(dd)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(ee)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(iii)
in sub-paragraph (c)—
(aa)
“(b)
the references to “certification” include a “certificate” as defined in these Regulations or an equivalent certificate published by an authority in another part of the United Kingdom under legislation in force there;”,
(bb)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(c)
in paragraph (12)—
(i)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(ii)
in sub-paragraph (b)(i)—
(aa)
“(ii)
in another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(bb)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to;”,
(cc)
“(b)
the references to “certification” include a “certificate” as defined in these Regulations or an equivalent certificate published by an authority in another part of the United Kingdom under legislation in force there;”,
(dd)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom
for co-ordinating the standards and methods of diagnosis referred to.”,
(ee)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(iii)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(d)
in paragraph (14)—
(i)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(ii)
in sub-paragraph (b)(ii)—
(aa)
“(ii)
in another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(bb)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to;”,
(cc)
“(b)
the references to “certification” include a “certificate” as defined in these Regulations or an equivalent certificate published by an authority in another part of the United Kingdom under legislation in force there;”,
(dd)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(ee)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(iii)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(e)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(f)
in paragraph (16)—
(i)
“(i)
the reference to “competent authority” includes the authority of another part of the United Kingdom which approves accommodation for the purpose of that period of quarantine, in accordance with legislation in force in that part of the United Kingdom;”,
(ii)
in sub-paragraph (b)(iv)—
(aa)
“(bb)
in relation to another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(bb)
“(bb)
in relation to another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(cc)
“(bb)
in another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(dd)
“(bb)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to;”,
(iii)
in sub-paragraph (c)(ii)—
(aa)
“(ii)
in another part of the United Kingdom, an equivalent authority under legislation in force in that part of the United Kingdom;”,
(bb)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to;”,
(cc)
“(b)
the references to “certification” include a “certificate” as defined in these Regulations or an equivalent certificate published by an authority in another part of the United Kingdom under legislation in force there;”,
(dd)
“(ii)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”,
(ee)
“(b)
in relation to another part of the United Kingdom, a laboratory approved by an authority under legislation in force in that part of the United Kingdom,
for co-ordinating the standards and methods of diagnosis referred to.”.
(4)
In regulation 33 (amendment of the Equine Animal (Identification) (Scotland) Regulations 2019)—
(a)
in paragraph (2), for the substituted text substitute “Great Britain from a third country”,
(b)
in paragraph (4), for the substituted text substitute “Great Britain from a third country”,
(c)
“(5)
Omit regulation 19(1)(c).”,
(d)
in paragraph (6)—
(i)
in sub-paragraph (a)—
(aa)
for “Union” substitute “the Union”,
(bb)
for “United Kingdom” substitute “Great Britain”,
(ii)
in sub-paragraph (b)—
(aa)
for “Union” substitute “the Union”,
(bb)
for “United Kingdom” substitute “Great Britain from a third country”,
(iii)
in sub-paragraph (d) for “the United Kingdom” substitute “Great Britain”.
Amendment of the Official Controls (Agriculture etc.) (Scotland) Regulations 20194.
(1)
(2)
In regulation 2 (interpretation)—
(a)
for “EU Regulation” in each place where it occurs substitute “Official Controls Regulation”,
(b)
in paragraph (1), in the definition of “relevant legislation” omit “European and domestic”.
(3)
In regulation 4 (disclosure of information)—
(a)
omit “ in the United Kingdom and other member States”,
(b)
for “EU Regulation” substitute “Official Controls Regulation”.
(4)
In regulation 5(1) (powers of auditors), for “EU Regulation” substitute “Official Controls Regulation”.
(5)
In regulation 7(1) (powers of Food Standards Scotland undertaking audits), for “EU Regulation” substitute “Official Controls Regulation”.
(6)
In regulation 9 (facilitating assistance and co-operation)—
(a)
in paragraph (1), omit “of another member State” in both places where it occurs,
(b)
omit paragraph (2),
(c)
in paragraph (3), for “EU Regulation” substitute “Official Controls Regulation”.
(7)
In regulation 11 (enforcement and prosecution), for “EU Regulation” in both places where it occurs substitute “Official Controls Regulation”.
(8)
In regulation 12(1) (powers of enforcement officers), for “EU Regulation” in both places where it occurs substitute “Official Controls Regulation”.
(9)
In regulation 13 (powers of entry), for “EU Regulation” in each place where it occurs substitute “Official Controls Regulation”.
St Andrew’s House,
Edinburgh
These Regulations are made principally in exercise of the powers conferred by paragraphs 1(1) and (3) of schedule 2 and paragraph 21(b) of schedule 7 of the European Union (Withdrawal) Act 2018. These Regulations address failures of retained EU law to operate effectively and other deficiencies arising from the withdrawal of the UK from the European Union.
Regulation 2 is made in exercise of powers under the European Communities Act 1972, and amends the definition of “qualification certificate” in the Welfare of Animals at the Time of Killing (Scotland) Regulations 2012 to update the list of qualification authorities who issue qualification certificates that are recognised in Scotland for the purposes of obtaining a certificate of competence. This amendment comes into force immediately before IP completion day.
Regulation 3 is made in exercise of powers under the European Union (Withdrawal) Act 2018, and makes amendments to the Animal Health (EU Exit) (Scotland) (Amendment) Regulations 2019, which in turn make amendments to secondary legislation in the field of animal health. These amendments to the Animal Health (EU Exit) (Scotland) (Amendment) Regulations 2019 are required so as to prevent, remedy or mitigate deficiencies arising from the withdrawal of the United Kingdom from the European Union. These amendments come into force immediately before IP completion day.
Regulation 4 is made in exercise of powers under the European Union (Withdrawal) Act 2018, and makes amendments to the Official Controls (Agriculture etc.) (Scotland) Regulations 2019 in order to prevent, remedy or mitigate deficiencies arising from the withdrawal of the United Kingdom from the European Union. These amendments come into force on IP completion day.
No business and regulatory impact assessment has been prepared for these Regulations as no impact upon business, charities or voluntary bodies is foreseen.