GMC Guidance on Informed Consent
Bulletin of Medical Ethics 1999 February; (145): 4-6
Showing items related by title, author, creator and subject.
Guidance for Institutional Review Boards, Clinical Investigations, and Sponsors: Exception From Informed Consent Requirements for Emergency Research: Draft Guidance Unknown author (United States. Food and Drug Administration [FDA], 2006-07)
Guidance on Informed Consent of in Vitro Diagnostic Device Studies Using Leftover Human Specimens That Are Not Individually Identifiable Unknown author (United States. Food and Drug Administration [FDA]. Center for Devices and Radiological Health. Office of In Vitro Diagnostic Device Evaluation and SafetyCenter for Biologic Evaluation and Research. Office of Blood Research and Review, 2006-04-25)