See All Resources

Comments to Docket 2006-D-0031, Draft Informed Consent Information Sheet: Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors (Public Comments)

Comments provided on: September 11, 2014

Comments provided to: Food and Drug Administration

• Comments to Docket 2006-D-0031, Draft Informed Consent Information Sheet: Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors (Public Comments)