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Human Subjects Division

Learn more about the Accreditation Process for the UW Human Research Protection Program at HSD name=

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For IRB Members
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For IRB Members

Frequently Used Resources & References
» HHS/OHRP – IRB Guidebook
» FDA – Guidance for IRBs
» PRIM&R
» IRB Forum
» Consent Form Checklist - 12/07/05 (doc) 58 kb

New to the IRB
» IRB Application Life Cycle
» Belmont Report
» HRSA Online Training: Protecting Human Subjects
 

 

Commonly Cited Regulatory Sections
46.109 IRB review of research.
46.111 Criteria for IRB approval of research.
46.116 General requirements for informed consent.
46.117

Documentation of informed consent

46.123 Early termination of research support: Evaluation of applications and proposals.
Subpart B Additional Protections for Pregnant Women, Human Fetuses and Neonates Involved in Research
Subpart C Additional DHHS Protections Pertaining to Biomedical and Behavioral Research Involving Prisoners as Subjects
Subpart D Additional DHHS Protections for Children Involved as Subjects in Research