OpenLegislation

Part 9 Post-authorisation safety studiesF1

  1. 28Scope and interpretation
  2. 29Obligations as to post-authorisation safety studies
  3. 30Format of the study protocol
  4. 31Format of the abstract of the final study report
  5. 32Format of the final study report

Annotations

Textual amendments

F1

Sch. 12A inserted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 6 (as amended by S.I. 2019/1385, reg. 1, Sch. 1 para. 9 and S.I. 2020/1488, reg. 1, Sch. 2 para. 192); 2020 c. 1, Sch. 5 para. 1(1)