[F1Principles based on Articles 2 to 5 of the GCP DirectiveU.K.
4. The necessary procedures to secure the quality of every aspect of the trial shall be complied with.]
Textual Amendments
F1Sch. 1 Pt. 2 substituted (29.8.2006) by The Medicines for Human Use (Clinical Trials) Amendment Regulations 2006 (S.I. 2006/1928), regs. 1(1), 27(2)