OpenLegislation

Chapter 2 MARKETING AUTHORISATION REQUIREMENTSF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. 3Donation, procurement and testing
  2. 4Clinical trials
  3. 5Good manufacturing practice
  4. 6Issues specific to medical devices
  5. 7Specific requirements for advanced therapy medicinal products containing devices

Annotations

Textual amendments

F1

Regulation revoked (in so far as it applies to medicinal products for human use) (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 9 para. 1(o) (subject to transitional provisions in S.I. 2012/1916, Sch. 33A); 2020 c. 1, Sch. 5 para. 1(1)