FDA Guidance for Institutional Review Boards, Investigators, and Sponsors: Use of Electronic Informed Consent - Questions and Answers
Title:
FDA Guidance for Institutional Review Boards, Investigators, and Sponsors: Use of Electronic Informed Consent - Questions and Answers
Origin/Publisher:
FDA, http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM436811.pdf
Content:
This guidance is intended for institutional review boards (IRBs), investigators, and sponsors engaged in or responsible for oversight of human subject research under HHS and/or FDA regulations.