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Regulation 31 Amendment of Schedule 1I1

United Kingdom

(1)

Schedule 1 (further provisions for classification of medicinal products) is amended as follows.

(2)

In Part 1 M1 (descriptions of certain medicinal products to be available only on prescription), in paragraph 1—

(a)

omit “and” at the end of sub-paragraph (f);

(b)

insert “ ; and ” at the end of sub-paragraph (g); and

(c)

after sub-paragraph (g) insert—

“(h)

a product which is authorised by the licensing authority on a temporary basis under regulation 174, in circumstances where the licensing authority has attached a condition to that authorisation to the effect that, for the duration of the temporary authorisation, the product is classified as a prescription only medicine.”.

(3)

In Part 2 M2 (descriptions of certain medicinal products to be available only from a pharmacy), in paragraph 3—

(a)

insert “ ; and ” at the end of sub-paragraph (c); and

(b)

after sub-paragraph (c) insert—

“(d)

a product which is authorised by the licensing authority on a temporary basis under regulation 174, in circumstances where the licensing authority has attached a condition to that authorisation to the effect that, for the duration of the temporary authorisation, it is only to be available from a pharmacy.”.

Annotations

Marginal citations

M1

Part 1 has been amended by S.I. 2014/490 and 2019/775.

M2

Part 2 has been amended by S.I. 2019/775.

Commencement

I1

Reg. 31 in force at 6.11.2020, see reg. 1(2)