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There are currently no known outstanding effects for the The Human Medicines (Coronavirus and Influenza) (Amendment) Regulations 2020, Section 31.
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31.—(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.”.
Commencement Information
I1Reg. 31 in force at 6.11.2020, see reg. 1(2)
Marginal Citations
M1Part 1 has been amended by S.I. 2014/490 and 2019/775.
M2Part 2 has been amended by S.I. 2019/775.
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