PART 3Amendment of Part 3 (manufacture and distribution of medicinal products and active substances)

Amendment of Schedule 5 (review upon oral representations)I122

1

Schedule 5 M1 is amended as follows.

2

In paragraph 1(2)(e), 3(11)(b) and 5(2)(d) after—

a

“UK marketing authorisation,” in each place it appears, insert “ parallel import licence, ”; and

b

“an authorisation,” or “the authorisation,” in each place it appears, insert “ licence, ”.

3

In paragraph 3 omit sub-paragraph (11)(b)(iii).

4

In paragraph 5 omit sub-paragraph (2)(c).