Use of Electronic Informed Consent in Clinical Investigations – Questions and Answers: Guidance for Institutional Review Boards, Investigators, and Sponsors
Information
Type
Guidance
Regulated products
Biologics, Drugs, Medical Devices
Topics
Administrative / Procedural
Published
December 15, 2016
Last updated
January 26, 2021
Description
This document is a guidance document titled "Use of Electronic Informed Consent in Clinical Investigations – Questions and Answers". It falls under the topic of "Administrative / Procedural".
Tags
Organization
Country / Region
United States
License
Other (Public Domain)