Minutes of Institutional Review Board (IRB) Meetings: Guidance for Institutions and IRBs
Information
Type
Guidance
Regulated products
Biologics, Drugs, Medical Devices
Topics
Good Clinical Practice (GCP), Pediatric Product Development
Published
September 25, 2017
Last updated
April 11, 2024
Description
This document provides guidance for institutions and IRBs on conducting and documenting minutes of IRB meetings, focusing on Good Clinical Practice (GCP).
Tags
Organization
Country / Region
United States
License
Other (Public Domain)