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Â鶹Éç IRB Procedures Manual for the Â鶹Éç human subjects protections program and operations of the Â鶹Éç IRB prior to January 21, 2019.

Â鶹Éç IRB Guide for Researchers for any studies initially approved by the Â鶹Éç IRB before January 21, 2019.

Â鶹Éç IRB application review process flow chart.

Responsibilities of directors of research studies involving human subjects.

Â鶹Éç IRB guidance on information individuals in New Hampshire are legally required to report. Updated May 2026.

Â鶹Éç IRB HIPAA sample research authorization form.

Â鶹Éç IRB HIPAA sample authorization language for consent forms.

Â鶹Éç IRB guidance on HIPAA impacts on research Involving human subjects.

Â鶹Éç IRB guidelines for research involving children/minors. Updated April 2026.

NIH webpage on clinical trials