PPT-Which Projects Do – and do Not – Require IRB Review?

A Brief Overview of the Types of Projects Which Need IRB Oversight Back to Basics Anyone engaged in human subjects research at Emory is bound to comply with regulations and policies for protecting participants . Find us online. Information available online. IRB procedures and bylaws. IRB FAQs. Definition of research. Link to the CITI ethics training. Application form. Instructions to fill out the application form. Show the data.. Jeffery W. Rodamar. Workshop on Revisions to the Common Rule. In Relation to Behavioral and Social Sciences . National Research Council. March 21-22, 2013. . 1. Disclaimer . This presentation is intended to promote the exchange of ideas among researchers and policy makers. The views expressed in it are those of the author as part of ongoing research and analysis and do not necessarily reflect the position of the US Department of Education or any other Common Rule department or agency. . Agenda. GRU IRB Development and Changes. WIRB-Copernicus Group. Process for transfer of Chesapeake IRB protocols. Process for the new WIRB submissions. GRU IRB Development and Changes. WIRB and IRBNet. Micheal A. Kuhn, MD. Vice Chair, Loma Linda University. Institutional Review Board. What type of . research needs. IRB review?. Anything and everything . that involves human subjects. Navigating the IRB process. Susan Loess-Perez, MS, CIP, CCRC. Director of Research Compliance. Office of Research Services. Graduate Thesis and Dissertation Conference. February 6, 2016. Purpose of IRB. What Requires Review. Levels of Review. A How-To Guide. http://www.uthsc.edu/research/research_compliance/IRB. /. (901) 448-4824. irb@uthsc.edu. UTHSC Institutional Review . Board (IRB). Charged with protecting human research subjects. Ensures compliance with the federal regulations (DHHS, FDA, & HIPAA) with regards to research applications, consent forms and other research materials to be used; and with regards to the conduct of the research itself. May 19, 2017. Topics. Drivers for Centralized IRB Review. Regulatory changes . Trial Innovation Network. How JHM IRB will address the Single IRB requirements . Key Decisions. When JHM is serving as the IRB of Record. Presented by. Sonu Jose. https://www.uwec.edu/orsp/faculty-academic-staff/research-using-human-subjects/. Outline. What is IRB?. Types of IRB Review. IRB Application Procedure . Hila Berger, Director Research Integrity and Compliance. Mylka Biascochea, Compliance Coordinator IRB/IACUC. 1. Objectives . What is the Institutional Review Board (IRB) responsible for? And why?. What is Human subjects research?. Amy Krenzer, CIP, IRB Coordinator. Hila Berger, MPH, CIP, Research compliance Officer. 1. Objectives . What is the Institutional Review Board (IRB) responsible for? And why?. What is Human subjects research?. Human Research Protection Program. 357 Administration Building. 806-742-2064. Donna Peters. . Esther Lucey. . Rick Shupe. The Belmont Report. The guiding principles behind human subjects research. (now DLMP!). Erica C. Jonlin, PhD. ejonlin@uw.edu. . IRB Consultant. Department of Pathology. July 22, 2020. Institutional Review Boards (IRBs). An Institutional . Review Board (IRB) . is a . board, committee, or other group formally designated by an institution to review, to approve the initiation of, and to conduct periodic review of, . Mary Eckart, BS, CIP, VA Central IRB Manager . Mikaela Myers, MA , VA Central IRB Manager. Jessica Kroll, MA, CIP, VA Central IRB Administrator . Webinar Housekeeping. Recording. - This session is recorded, and the associated handouts will be available on ORPP&E’s Education and Training website within a week after the webinar.. An IRB . Infoshort. February 2014. FYIs. FYIs are notifications to the IRB regarding a specific research activity or event that does not invoke a standard protocol submission.. FYIs - 2. A variety of items are submitted to the IRB as For Your...