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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
Statement of Compliance    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 FormAdobe PDF

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