Point in time view as at 01/01/2022.
The Human Medicines Regulations 2012, Paragraph 29 is up to date with all changes known to be in force on or before 05 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.
29.—(1) After receiving the appropriate committee's report under paragraph 26 or 27 or notification under paragraph 28 the licensing authority must decide whether to [F1grant or refuse the application].U.K.
(2) If the appropriate committee gives a report under paragraph 26 or 27, the licensing authority must take that into account in making its decision.
(3) The licensing authority must notify the applicant or holder of—
(a)its decision; and
(b)any advice given to it by the appropriate committee and the reasons for that advice.
Textual Amendments
F1Words in Sch. 11 para. 29(1) substituted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), regs. 1, 63(8)(c); 2020 c. 1, Sch. 5 para. 1(1)
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