BioIRB Meeting Dates
Biomedical IRB meeting dates.
Current and archived Biomedical IRB Membership Rosters.
Learn more about Biomedical Research.
Biospecimen & Data Repositories
Learn more about Biorepositories including consent, management and policies.
Guidance on planned Emergency Research.
Investigational Drugs and Devices
Information and resources on Investigational New Drug application and Investigational Device Exemption.
Resources and templates on Investigator-Initiated Trials.
sIRB for Multi-Site Research
Learn about sIRB and common terms.
IRB Authorization Agreements
Agreements to which USC is a party.
Requesting USC IRB to Act as the IRB of Record
Information on serving as the lead PI for a multi-site study.
Requesting USC to Cede Review
Information on being a PI that will rely on another IRB for review.
Clinical Research Coordinators
Resources for Clinical Research Coordinators.
Clinical Trial Basics
Learn more about Clinical Trials.
Complaints, Concerns and Report of Misconduct
Information on how to report human participants research related complaints, concerns, recommendations, or reports of misconduct.