OHRP, FDA Announce Availability of Guidance on Institutional Review Board Meetings

Summary

The Office for Human Research Protections (OHRP) and the Food and Drug Administration (FDA) have released a guidance document titled 'Minutes of Institutional Review Board Meetings; Guidance for Institutions and Institutional Review Boards' to assist institutions and IRBs in preparing and maintaining minutes of IRB meetings that meet FDA and HHS regulatory requirements.