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About Us
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IRB Policies and Procedures
Download Policies and Standard Operating Procedures
Forms:
Download application form for Administrative Committee approval (to be obtained from GS Office)
Format for reporting adverse events
Format for Submitting Final Report for Interventional Studies
Format for submitting Final Report for studies of Diagnostic Test Accuracy
Format for submitting Final Report for Observational (Case Control, Cohort, Cross Sectional) Studies
Format for submitting Final Report for other Study Designs
Format for submitting protocol amendments
NIH Format for DSMB report
ICMR Material Transfer Agreement Form
Format for IRB Reviewer checklist
Draft format for Informed Consent
Draft format for Tissue Banking
Checklist for Projects involving Artificial Intelligence (AI)/Machine Learning (MI) development/utilization
The New Drugs and Clinical Trial Rules 2019
Format for the annual report of the studies approved by the Institutional Review Board
Last updated on July 8, 2025
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