MRC guidelines for good clinical practice in clinical trials 1998 (withdrawn)

These guidelines apply to Medical Research Council (MRC) trials involving human participants and the administration of a treatment or type of management.



MRC Guidelines for Good Clinical Practice in Clinical Trials (PDF)

, 557 KB

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The guidelines include:

  • principles of good clinical practice
  • the role of MRC
  • the role of the host institution
  • the principal investigator and participating investigators
  • independent supervision of the trial
  • documentation
  • quality assurance and audit.

Page last updated: 8 November 2021

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