Point in time view as at 01/01/2022.
The Human Medicines Regulations 2012, Paragraph 15 is up to date with all changes known to be in force on or before 04 May 2025. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations.
15. The provisions of this Part are standard provisions of a manufacturer's licence relating to the import of medicinal products [F1from—U.K.
(a)in the case of an import into Great Britain, a country other than Northern Ireland or a country other than an approved country for import, or
(b)in the case of an import into Northern Ireland, a country other than an EEA State].
Textual Amendments
F1Sch. 4 para. 15(a)(b) substituted for words in Sch. 4 para. 15 (31.12.2020) by S.I. 2019/775, reg. 20(4) (as substituted by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1488), reg. 1, Sch. 2 para. 14(d))
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