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Schedule 3 PARTICULARS AND DOCUMENTS THAT MUST ACCOMPANY A REQUEST FOR APPROVAL, A MODIFICATION REQUEST AND A NOTIFICATION OF THE CONCLUSION OF A TRIALF1

  1. A1REQUEST FOR APPROVAL
  2. 1APPLICATION FOR ETHICS COMMITTEE OPINION
  3. 2REQUEST FOR AUTHORISATION
  4. 3MODIFICATION REQUEST
  5. 4NOTIFICATION OF CONCLUSION OF A CLINICAL TRIAL

Annotations

Textual amendments

F1

Words in Sch. 3 heading substituted (28.4.2026) by The Medicines for Human Use (Clinical Trials) (Amendment) Regulations 2025 (S.I. 2025/538), regs. 1(2), 39(2)