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Section 3 Minimum requirements for the quality systems for the performance of pharmacovigilance activities by national competent authorities and the AgencyF1

United Kingdom

Original text. Later amendments are not shown.

  1. 14Management of human resources
  2. 15Compliance management
  3. 16Record management and data retention
  4. 17Audit

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)