GMC Guidance on Good Standards
BULLETIN OF MEDICAL ETHICS 1995 April; 107: 4
Showing items related by title, author, creator and subject.
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EEC Note for Guidance: Good Clinical Practice for Trials on Medicinal Products in the European Community Unknown author (European Economic Community. Committee for Proprietary Medicinal Products. Working Party on Efficacy of Medicinal Products, 1991)
Guidance for Industry: Good Reprint Practices for the Distribution of Medical Journal Articles and Medical or Scientific Reference Publications on Unapproved New Uses of Approved Drugs and Approved or Cleared Medical Devices Unknown author (United States. Department of Health and Human Services. Food and Drug Administration [FDA]. Office of the Commissioner, Office of Policy, 2009-01)