Irb.duhs.duke.edu

Duke Health Institutional Review Board

WebDuke University Health System Institutional Review Board. Our mission ~ to ensure the protection of human research subjects by conducting scientific and ethical review of …

Actived: 6 days ago

URL: https://irb.duhs.duke.edu/

PERMISSIBLE RESEARCH-RELATED ACTIVITIES PRIOR TO IRB …

Web2 The following research-related activity may occur after the date of IRB review and before IRB approval is issued: • Site initiation visit (SIV) No amendments to a …

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Training & Resources Duke Health Institutional Review Board

WebPlease note: Duke Health researchers must renew their CITI modules every 3 years in order to be certified in Human Subjects Protection (HSP) training. DOCR CITI Training Support …

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IRB Members Duke Health Institutional Review Board

WebIRB members represent a diverse set of perspectives and expertise appropriate to the many kinds of research conducted at Duke. Our IRB members are physicians, researchers, …

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Policies Duke Health Institutional Review Board

WebThis policy describes the requirements for a study team member to conduct the consent process in a research study over which the DUHS Institutional Review Board (IRB) …

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Getting Started Duke Health Institutional Review Board

WebAll Duke Health researchers must complete the following required training before they are placed on a protocol submitted to the Duke Health IRB, and before they can submit in …

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Quality Improvement (QI) vs. Research (Policy and Checklist)

WebThis policy describes the key differences between Quality Improvement (QI) activities in health care versus research involving human subjects. The end of the policy …

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Federal Wide Assurance (FWA) Duke Health Institutional Review …

WebThen you will see a list of the "Duke U Hlth System, Inc." boards (they are numbered 1 through 10), and the IRB Registration Number for each board is located in the far left …

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iRIS Duke Health Institutional Review Board

WebPlease navigate to the DOCR iMedRIS Support Page.. Please note the iRIS FAQs are under the section "iRIS Tip Sheets and Job Aids" on the DOCR iMedRIS Support Page.. For …

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Contact Us Duke Health Institutional Review Board

WebFor help with iRIS: Chat with the DHTS Service Desk for Help, or submit a Self-Service Ticket (24/7) Phone Support for iRIS help: (919) 684-2243 (Press 4 for Research …

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NIH Implementation of the Revised Common Rule Provision …

WebThe National Institutes of Health (NIH) is informing the research community of its implementation of a provision in the 2018 Requirements for the Federal Policy for the …

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Consent Duke Health Institutional Review Board

WebOn the consent form, along with the label or stamp that is placed in the top right corner and contains the participant’s legal name (i.e. name matching with the DUHS medical …

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AMENDMENTS TO PREVIOUSLY APPROVED RESEARCH

Web11/22/2023. The Duke University Health System Institutional Review Board (DUHS IRB) requires that principal investigators promptly report to the IRB proposed changes in a …

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DE-IDENTIFICATION OF HEALTH INFORMATION SUBJECT TO …

Web1 DUKE UNIVERSITY HEALTH SYSTEM Human Research Protection Program . DE-IDENTIFICATION OF HEALTH INFORMATION SUBJECT TO THE …

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POLICY STATEMENT REGARDING THE IRB APPROVAL STAMP …

Web11/20/2023. The Duke University Health System Institutional Review Board (DUHS IRB) has determined that study subjects will review and sign a consent form that does not bear an …

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QUALITY IMPROVEMENT ACTIVITIES IN HEALTH CARE …

Web1 DUKE UNIVERSITY HEALTH SYSTEM Human Research Protection Program QUALITY IMPROVEMENT ACTIVITIES IN HEALTH CARE VERSUS …

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Research Subject to the Duke University health system

Web2 course of an event or crisis that threatens public health (including natural or man-made disasters). (3) Collection and analysis of information, biospecimens, or …

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THE PRIVACY RULE (“HIPAA”) IN RESEARCH

Web1 DUKE UNIVERSITY HEALTH SYSTEM Human Research Protection Program THE PRIVACY RULE (“HIPAA”) IN RESEARCH 11/20/2023 I. OVERVIEW The …

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Pregnant Partner Policy and Template Information Form

WebNovember 6, 2014. The DUHSIRB has posted a new policy regarding male research subjects’ partners who become pregnant while the male subject is involved in a research …

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Informed Consent and its Documentation FINAL

WebInformed Consent. When required by the DUHS IRB, legally effective informed consent must be obtained for every participant on every research study …

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