Institutional Review Board (IRB) Written Procedures: Guidance for Institutions and IRBs
Information
Type
Guidance
Regulated products
Biologics, Drugs, Medical Devices
Topics
Good Clinical Practice (GCP)
Published
May 17, 2018
Last updated
September 29, 2023
Description
A guidance document providing written procedures for Institutional Review Boards (IRBs) and institutions, focusing on Good Clinical Practice (GCP).
Tags
Organization
Country / Region
United States
License
Other (Public Domain)