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We promote the rights, safety and welfare of human research participants

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All that you need to know about Informed Consent

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Latest news

New Tools Available: Study Self-Audit Tool and CITIHub

OHSRP is pleased to announce two new tools designed to support study management and regulatory compliance.
- June 18, 2026
- process update
Guidance on submitting IND safety reports to the IRB

All IND safety reports must be submitted to the IRB per FDA guidance.
- April 21, 2026
- process update
New information on OHSRP website

The OHSRP website has been updated with several new resources and tools to support your work. We regularly update our website—please bookmark the hom…
- March 24, 2026
- website update

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Upcoming Events

NIH IRB Meeting
- Thursday, Jun 18th, 11:00 AM - 12:30 PM
NIH IRB Meeting
- Tuesday, Jun 23rd, 9:00 AM - 10:30 AM
NIH IRB Meeting
- Tuesday, Jun 23rd, 1:00 PM - 2:30 PM

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We promote the safe and ethical conduct of human subjects research

Our principles:

providing timely, consistent and compliant reviews
educating our community
communicating effectively and responsively
collaborating with stakeholders

NIH Federalwide Assurance More about us

Full accreditation by Association for the Accreditation of Human Research Protection Programs, Inc.