Guidance Documents
OHRP Guidance Documents
IRB Knowledge of Local Research Context
General Guidance on the Use of Another Institution's IRB
Suitability of a Designated Institutional Review Board (IRB)
Local IRB Review of Multicenter Clinical Trials
IRB Registration and Assurance Filing Procedures - General Information
Filing Federalwide Assurances of Protection for Human Subjects, See Item 5
FDA Guidance Documents
FDA Guidance - Non-Local IRB Review
FDA Information Sheet: Cooperative Research
User Number: 614775
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