Participants
Information for Research Participants
Informed Consent
All that you need to know about Informed Consent
NIH IRB Members
Information for NIH IRB Members
Common topics
Latest news
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Studies approved to enroll adults who lack decision-making capacity must include a protocol plan describing how assent will be obtained (or why assen…
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OHSRP is pleased to announce two new tools designed to support study management and regulatory compliance.
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All IND safety reports must be submitted to the IRB per FDA guidance.
Upcoming Events
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NIH IRB Meeting
- Tuesday, Aug 4th, 9:00 AM - 10:30 AM
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NIH IRB Meeting
- Tuesday, Aug 4th, 1:00 PM - 2:30 PM
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NIH IRB Meeting
- Wednesday, Aug 5th, 10:00 AM - 11:30 AM