The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 No. 775

PART 2 U.K. Amendment of Part 1 (General)

Amendment of Schedule 1 (further provisions for classification of medicinal products) U.K.

[F1 8.   In Schedule 1—

(a) in paragraph 1—

(i) in sub-paragraph (b), insert “UK” before “marketing authorisation”;

(ii) in sub-paragraphs (e)(i), (f)(i) and (g)(i), for “marketing authorisation” substitute “UK marketing authorisation, EU marketing authorisation, Article 126a authorisation or parallel import licence”; and

(b) in paragraph 4, for “marketing authorisation” substitute “UK marketing authorisation, EU marketing authorisation, Article 126a authorisation, parallel import licence”.]

Textual Amendments

F1 Reg. 8 substituted (31.12.2020 immediately before IP completion day) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1488), reg. 1, Sch. 2 para. 5