The Medicines for Human Use (Clinical Trials) Regulations 2004

Principles based on International Conference on Harmonisation GCP Guideline(1)

13.  Systems with procedures that assure the quality of every aspect of the trial shall be implemented.

(1)

See Section 2 of the Note for Guideline on Good Clinical Practice (CPMP/ICH/135/95) published by the European Agency for the Evaluation of Medicinal Products in July 2002.