The sIRB policy was established to accelerate the ethical review of non-exempt human research through a single Institutional Review Board and reduce inefficiencies. The NIH sIRB policy applies to intramural multi-site studies submitted for initial review after January 25, 2018. SMART IRB is a result of the collaboration between CTSA Program hubs to develop a Common Reciprocal Institutional Review Board Authorization Agreement (SMART IRB Agreement) to help facilitate the NIH single IRB (sIRB) policy. SMART IRB, which stands for the "Streamlined, Multisite, Accelerated Resources for Trials," was designed to streamline the IRB review process for multisite studies. The study teams who carry out human research.Comprehensive Cancer Center Protocol Review Committee.Institutional Conflict of Interest Office.The HRPP consists, in part, of: Wake Forest: In addition, the HRPP oversees the conduct of research projects to ensure ongoing compliance with the approved protocol, federal regulation, state and local laws, and institutional policy. The Human Research Protection Program (HRPP) serves participants in human research by coordinating the safety, ethics and regulatory reviews of research projects. Wake Forest University Health Sciences operates with eight biomedical Institutional Review Boards that are supported by the IRB Office. The Institutional Review Board (IRB), part of the Human Research Protection Program, reviews all research involving humans to ensure that participants are informed of all known risks posed by a research study and that these studies are conducted in accordance with the ethical standards put forward by the Belmont Report, and federal, state, and local regulations, and policies governing human research.
See All Programs, Short Courses, Seminars, etc.Medical Student Research Program (MSRP).Academic Learning Health System Scholars Program.Investigator New Drug (IND)/Investigational Device Exemptions (IDE).
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