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Revised Common Rule

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Revised Common Rule

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  1. To start the presentation, click on this button in the lower right corner of your screen. The presentation will begin after the screen changes and you press enter. Developed by: U-MIC

  2. Revised Common Rule Effective January 21, 2019 Developed by: U-MIC University of Michigan IRB Collaborative

  3. Common Rule • 45 CFR 46 subpart A • Department of Health and Human Services (HHS) • investigators conducting research involving human subjects • IRBs • 2018 revision • implementation date: January 21, 2019 • New studies with federal funding • subject to all revised Common Rule requirements • At UM, new studies without federal funding • subject to all Common Rule provisions • except requirement to post consent materials to public website Revised Common Rule Developed by: U-MIC

  4. Common Rule revisions • apply only to • HHS requirements (45 CFR 46) • no bearing on • FDA requirements (21 CFR 50 and 56) • HIPAA requirements (45 CFR 164) Revised Common Rule Developed by: U-MIC

  5. Revised Common Rule • continuing review • exempt research • informed consent • other aspects of research Revised Common Rule Developed by: U-MIC

  6. Continuing review • no longer required for some minimal risk research • most studies that qualify for expedited review • other studies (expedited or convened-board review) if • all subject intervention/interaction complete • remaining activity confined to • final analysis of identifiable data or biospecimens • accessing follow-up clinical data • still required for studies subject to • FDA regulations • ICH-GCP E6 standards Revised Common Rule Developed by: U-MIC

  7. Exemptions • modification of existing categories • expansion of existing categories • addition of new categories • UM implementing only one • research involving only benign behavioral intervention • new exempt determination processes • limited IRB review • similar to expedited review • self-determination of exemption • PI may issue system-generated exemption determination letter • eResearch will indicate whether self-determination is permissible • permissible for some exempt research • notpermissiblefor research involving • HIPAA-covered component • for research subject to limited IRB review Revised Common Rule Developed by: U-MIC

  8. Informed consent • key information section • details most likely to assist in consent decision • new required elements • changes to waiver criteria and documentation • other process changes • broad consent • unspecified future use of identifiable data/biosopecimens • UM not implementing broad consent Revised Common Rule Developed by: U-MIC

  9. new required elements of consent • identifiable private information/biospecimens • whether identifiers may be removed • whether de-identified information/biospecimensmay be used/shared • use of biospecimens • whether biospecimens may be used for profit • whether subject will share in profit • clinically relevant results • whether results returned to subject • under what conditions • whole-genome sequencing • statement that research will/might include whole-genome sequencing Revised Common Rule Developed by: U-MIC

  10. IRBMED standard informed consent template • available on IRBMED website • complies with all revised Common Rule requirements • key information section • new required elements of consent Revised Common Rule Developed by: U-MIC

  11. New informed consent waiver provisions • use of identifiable private information/biospecimens • must explain why use of identifiers is necessary • use of identifiable information/biospecimens for recruitment • allowed under certain circumstances • waiver of consent no longer necessary • HIPAA authorization requirements may still apply. Revised Common Rule Developed by: U-MIC

  12. Public posting of approved informed consent materials • required for federally-sponsored clinical trials • after recruitment • no later than 60 days after last study visit • publicly available federal website • ClinicalTrials.gov • FederalRegister.gov Revised Common Rule Developed by: U-MIC

  13. Revised Common Rule Revised Common Rule Developed by: U-MIC

  14. Brian Seabolt IRBMED Thank you. Developed by: U-MIC

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