Institutional Review Board (IRB) Forms

Please go the to create amendments and CRs for all currently active IRB protocols. To begin a new protocol, please go to to begin the review process for the Clinical Science Evaluation Committee. For information on how to use eIRB, please visit

IRB Protocol Forms
Assent for Minors Form     Microsoft Word
IRB Consent Form Microsoft Word
Informed Consent for Genetic Testing     Microsoft Word
Informed consent for protocols using a Humanitarian Use Device     Microsoft Word
Human Tissue Section and Request Form     Adobe PDF
Use of Drugs or Biological Agents Form     Microsoft Word
Protocol Exception Request Form     Microsoft Word
Human Research Billing Analysis Form (HRBAF)    
All questions regarding this form should be directed to the Office of Billing Compliance at (646) 962-7539
Microsoft Excel
QA/QI Form New 7/6/2017
Please submit this completed form to
Adobe PDF

Immediate Reporting
WCMC Immediate Reporting Policy and FAQ     Go to Policy and FAQ
Immediate Reporting Form     Microsoft Word
Adverse Event & IND Safety Reporting Cumulative Table     Microsoft Word

Financial Disclosure
Study Specific Report – Internal WCMC Use
(formerly the Study Specific Financial Disclosure)
Information & Help
Web Application
Study Specific Report – External Non-WCMC Use     Information and Forms
Guidance for Conflicts of Interest in Informed Consent Form Adobe PDF

Pathology Review - General Information     Adobe PDF
Pathology Review - FAQ     Adobe PDF
Pathology Review Instructions     Adobe PDF