PPT-VA Central IRB Annette Anderson, MS, CIP

VA Central IRB Administrator Updated March 27 2017 Purpose of VA Central IRB Primary Purpose Improve human research protections in VA multisite studies by ensuring Consistent expert ethical and scientific review. freespiritfabriccom Copyright 2013 All rights reserved brPage 2br wwwfreespiritfabriccom Copyright 2013 All rights reserved Finished quilt size 60 x 68 1524cm x 17272cm Fabric Requirements Note WOF Width of Fabric Fat quarters of PWAT 084CRE PWAT 08 An IRB . Infoshort. June 2014. Working Definition . A central IRB is one that serves as IRB of record for all of the sites engaged in a research study . All institutions involved in the study have developed an agreement ceding IRB review responsibility to the central IRB. Overview of Today’s presentation . How do I know if I am using VA Resources? . What are the VA training requirements? . What do I do if I am storing PHI at my UI office?. Record retention policy . SLSQ v12-8-11. What is ‘IRB Awareness’ . Many of our Bronze Medallion members are asked to assist with the manual handling and set up/pack down of IRBs when on . patrol. It is important that these members know how to operate safely around IRB equipment if/when asked to help by the IRB . General Procedures for Ceding IRBMED Oversight. Procedures Specific to Chesapeake IRB. Medical School. Institutional Review Board (IRBMED). Introductions . Representatives. . Chesapeake. . IRBMED. Medical School. Lessons Learned. NISO Forum. Annette Bailey. Virginia Tech. My Experience with Open Source. LibX. Browser plug-in that includes a toolbar, context menu and embeds library resources into web pages. LibX Edition Builder. 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. Kevin L. Nellis, MS, CIP. Executive Director, Human Research Protections and Quality Assurance. Criteria for IRB Approval (111 Findings). 2. Risks . to . research participants are . minimized; . Risks . 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. . Objectives. Why are renewals necessary?. What projects require a renewal?. How do I find the form?. How do I . fill . out the form. ?. What are the required documents with submission?. When do I submit the renewal?. Janet G. Lenz, Ph.D.. Gary W. Peterson, Ph.D. .. Robert C. Reardon, Ph.D.. James P. Sampson, Jr., Ph.D.. Florida State University. Denise E. Saunders, Ph.D.. Private Practice. National Career . Development Association, June . 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?. 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..