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)
• Protection of Human Subjects; Standards for Institutional Review Boards for Clinical Investigations 

  Unknown author (United States. Department of Health and Human Services. Food and Drug Administration, 1981-02-27)
• Protection of Human Subjects; Informed Consent; Standards for Institutional Review Boards for Clinical Investigations. Proposed Rule 

  Unknown author (United States. Food and Drug Administration, 1988-11-10)