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 creator (United States. Department of Health and Human Services.[HHS] Food and Drug Administration [FDA], 1981-01-27)
• Protection of Human Subjects; Informed Consent; Standards for Institutional Review Boards for Clinical Investigations. Proposed Rule 

  Unknown creator (United States. Food and Drug Administration, 1988-11-10)
• Protection of Human Subjects; Informed Consent; Standards for Institutional Review Boards for Clinical Investigation. Final Rule 

  Unknown creator (United States. Food and Drug Administration, 1991-06-18)