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

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

[F18.  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”.]