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Office for Human Research Protections

CITI Training & National Institutes of Health (NIH)

OHRP Homepage Expedited Review Categories Exempt Review Categories (45 CFR 46.101(b)) Federal Regulations: DHHS - Code of Federal Regulations (45 CFR 46) FDA - Good Clinical Practice Program (formerly FDA 21 CFR 50 & FDA 21 CFR 56) Decision Charts Federalwide Assurance Search Assurance Registration Tips on Informed Consent The Belmont Historical Archive The Belmont Report

IRBNet This is the website where you will submit all documentation to the IRB. Please note that as of September 1, 2008, hard copies are no longer accepted by the IRB. Mandatory Training through CITI Earn a certificate that must be submitted with your IRB application.  Please see our CITI FAQ page for complete details. As of fall 2008, all investigators, co-investigators, sponsor/advisors and research assistants must complete training. Please note that If you have been funded through NIH,  you will need to complete CITI AND NIH training courses. Investigator Training (NIH)   Nuremberg Code  Office of Human Subject Research

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