WebFeb 4, 2024 · HRPP Operations Manual, Part 5, Section IV A. Federally-funded cooperative (i.e, "multi-site") human research studies are required per the Common Rule (45 CFR 46.114) to utilize a single IRB-of-Record (sIRB) to streamline the review process for human participant protections and to avoid duplicate review by an institutional review board at … WebApr 7, 2024 · Expand the tab “University of Minnesota Courses.”. Click “Add a Course.”. Select the training required by or most appropriate to your research activities. Click …
Ethics & Compliance - University of Michigan
WebMar 15, 2024 · eResearch is U-M's site for electronic research administration. Access: Regulatory Management (for IRB or IBC rDNA applications); Proposal Management (eRPM) for the e-routing, approval, and submission of proposals (PAFs) and Unfunded Agreements (UFAs) to external entities); and Animal Management (for IACUC protocols and ULAM). WebAn external investigator submitting to UC Davis IRB for review under a reliance agreement may complete one of the following to meet the basic human research protections training requirement:. The human subjects protection training required by the investigator’s home institution.; UCD CITI human subjects protection training. External investigators may … cuisance transfer market
IRB Training Division of Research
WebReference Materials. See the Reference Materials page for step-by-step instructions and support materials on using eResearch Regulatory Management. ITS Service Center. Monday 5–6 a.m. Saturday 3–9 a.m. Saturday 11 p.m.–Sunday 7 a.m. WebUniversity of Michigan faculty, ... courses for either biomedical or social-behavioral human subjects protections from the Collaborative Institutional Training Initiative (CITI). The … WebTraining for Research Administrators Research Administrators (RAs) generally are not required to take PEERRS courses. However, the offices of Research and Sponsored … eastern new england commissioner college