Informed Consent in Clinical Investigations
Lachin, John M.
Biometrics 1977 December; 33(4): 761-762
Showing items related by title, author, creator and subject.
Protection of Human Subjects; Informed Consent; Standards for Institutional Review Boards for Clinical Investigations; and Clinical Investigations Which May Be Reviewed Through Expedited Review Procedure Unknown author (United States. Department of Health and Human Services.[HHS] Food and Drug Administration [FDA], 1981-01-27)
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Boards, Clinical Investigations, and Sponsors: Exception From Informed Consent Requirements for Emergency Research: Draft Guidance Unknown author (United States.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)