OpenLegislation

Division 11 F1

United Kingdom

Original text. Later amendments are not shown.

Management and reporting of adverse events/adverse reactions and other medically important events while the study is being conducted.

Annotations

Textual amendments

F1

Regulation revoked in part (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 9 para. 1(t) (subject to transitional provisions in S.I. 2012/1916, Sch. 33A); 2020 c. 1, Sch. 5 para. 1(1)