Human Research Protections

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Institutional Policies & Procedures

WCM Human Research Protections Standard Operating Policies

001.1 IRB Review of Research Subject to the 2018 Common Rule.pdf

230.00 Human Research Protections Program.pdf

101.1 Delegation of Authority.pdf

200.1 Staff Processing of Submissions.pdf

201.1 Exempt Review.pdf

202.1 Initial Expedited Review.pdf

203.1 Initial Full Board Review.pdf

230.04 Changes to Approved Research.pdf

205.1 Continuing Review.pdf

206.1 Study Closure.pdf

207.1 IRB Meeting Conduct.pdf

230.02 Reports and Investigations of Research Non-Compliance

230.05 Protocol Violations and Deviations

230.06 IRB Reliance Process and Single IRB

230.07 Principal Investigator Eligibility

300.1 Research Supported by the Department of Defense

Policies Under Review

Immediate Reporting Policy

Official Memoranda

Aug. 4, 2023: Change to IRB Stamping of Single/Central IRB-acknowledged Informed Consent Forms
Undated, 2021: Process Clarification: Requests for IRB Roster/Membership Information
Feb. 2, 2021: SARS-CoV-2 Vaccination Considerations for Clinical Research Studies
Feb. 2, 2021: Remote Monitoring for Clinical Studies
April 1, 2019: Process Clarification: Approval Stamps for IRB-approved Documents

Contact Us IRB Member Portal Forms, Templates & Guidelines Request a Consultation WCM/CUMC Collaborations

Weill Cornell Medicine Human Research Protections 575 Lexington Avenue New York, NY 10022 Phone: (646) 962-8200