Memo 03.01.13 Extended Medical Approval Memo to Researchers from Ann Arvin Categories: Regulatory Compliance March 1, 2013 Dear Colleagues: The Research Compliance Office is implementing a new procedure to streamline the review process and reduce administrative burden on researchers, while still affording protections to human subjects. Effective March 1, 2013, the IRBs will discontinue annual renewal of chart review protocols that involve minimal risk non-federally sponsored human subject research until the end of year three of ongoing research. Rather than an annual renewal, chart review …
June 11, 2026
