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12.—(1) Schedule 1 (further provisions for classification of medicinal products) is amended as follows.
(2) In Part 1(1) (descriptions of certain medicinal products to be available only on prescription), in paragraph 1—
(a)omit “and” at the end of sub-paragraph (g);
(b)insert “; and” at the end of sub-paragraph (h); and
(c)after sub-paragraph (h) insert—
“(i)an EAMS medicinal product, in circumstances where the licensing authority has attached a condition to the EAMS scientific opinion in respect of that product to the effect that, for the duration of that opinion, the product is classified as a prescription only medicine.”.
(3) In Part 2(2) (descriptions of certain medicinal products to be available only from a pharmacy), in paragraph 3—
(a)omit “and” at the end of sub-paragraph (c);
(b)insert “; and” at the end of sub-paragraph (d); and
(c)after sub-paragraph (d) insert—
“(e)an EAMS medicinal product, in circumstances where the licensing authority has attached a condition to the EAMS scientific opinion in respect of that product to the effect that, for the duration of that opinion, it is only to be available from a pharmacy.”.
Amended by S.I. 2014/490, 2019/775 and 2020/1125.
Amended by S.I. 2019/775 and 2020/1125.
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