Responsibilities of Institutions and Central IRBs for Multicenter Clinical Trial Protocols*.
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Abbreviations: IRB, institutional review board; FDA, Food and Drug Administration; FWA, federalwide assurance; HIPAA, Health Insurance Portability and Accountability Act; OHRP, Office of Human Research Protections.*This table provides highlights of a guide for institutions that can help to decouple institutional and IRB responsibilities to assist in the acceptance of centralized ethical review; the detailed guide is provided in Appendix S1.
创建时间：
2015-12-02
