New England Institutional Review Board - NEIRB - A National Central IRB - Regulatory References
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Regulatory References
Please use the links below to access regulatory information:
21 CFR 50 (Informed Consent)
21 CFR 56 (Institutional Review Boards)
21 CFR 312 (Investigational New Drug Application)
21 CFR 812 (Investigational Device Exemption)
45 CFR 46 (OHRP Protection of Human Subjects)
The Belmont Report
ICH (International Conference on Harmonisation)
FDA Information Sheet Guidances
85 Wells Avenue Suite 107 Newton, MA 02459
Phone: 617-243-3924 Fax: 617-969-1310
info@neirb.com
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