Business · 15/12/2016Updated: 10/17/2026 · 1 min read
FDA and HHS Announce Availability of Guidance on Electronic Informed Consent
Summary
The FDA and OHRP have released a guidance document addressing the use of electronic systems for informed consent in human subject research, primarily for HHS-regulated studies and FDA-regulated clinical investigations.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →