Frequently Asked Questions - IRB Registration: Guidance for Institutional Review Boards (IRBs)
Information
Type
Guidance
Regulated products
Biologics, Drugs, Medical Devices
Topics
Good Clinical Practice (GCP)
Published
July 9, 2009
Last updated
July 21, 2021
Description
A guidance document for Institutional Review Boards (IRBs) on Good Clinical Practice (GCP) and frequently asked questions about IRB registration.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)