Paragraph 2 F1

This Schedule applies to a veterinary medicinal product which is—

(a)

a qualifying Northern Ireland good in respect of which there is a marketing authorisation valid in Northern Ireland under the Northern Ireland VMRs,

(b)

not a product in respect of which there is a marketing authorisation which is valid in Great Britain (including any marketing authorisation which has effect under paragraph 3 of Schedule 1A),

(c)

not a product in respect of which a QNIG certificate issued under this Schedule already applies, and

(d)

not a product to which Article 41(1) of the EU withdrawal agreement applies.

Annotations

Textual amendments

F1: Sch. 1B inserted (E.W.S.) (31.12.2020) by The Veterinary Medicines and Residues (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1461), regs. 1(2)(b), 4(8)