PPT-Is this Research? Exempt? Expedited?

Vivienne Carrasco MPH CIP Senior IRB Regulatory Analyst Social amp Behavioral Sciences IRB Human Subject Research Office Assurance and Regulations The University of Miami requires review and approval by an IRB of all research involving human subjects if any UM faculty staff or students are engaged as key personnel in that research FWA Policy 24 Revised May 10 2011 conducted in accordance with its FWA binding agreement with DHHS OHRP and FDA when applicable. couts cagov New January 1 2011 Mandatory Form Code of Civil Procedure 63001 63010 Cal Rules of Court rules 31545 31552 This information sheet is for anyone involved in a civil lawsuit who is considering taking part in an expedited jury trial a trial An IRB . Infoshort. April 2013. Expedited Definition. Expedited review studies are those minimal risk protocols that do not need to be reviewed by the fully convened IRB (21 CFR 56.110; 45 CFR 46.110). DEMOGRAPHIC RESEARCH http://www.demographic-research.org/Volumes/Vol26/11/ DOI: 10.4054/DemRes.2012.26.11centenarians explained S. Percy Ivy, MD. Associate Chief, Senior Investigator. Investigational Drug Branch, National Cancer Institute. ivyp@ctep.nci.nih.gov. . National Cancer Institute. . . Cancer Therapy Evaluation Program (CTEP). Angela Bain, . IRB Administrator. abain@uga.edu. . 706-542-3821. IRB Protocol Types. 2. Not Human Subjects Research. Exempt . Expedited . Full Committee. Exempt Categories. Category 1: Research conducted in commonly accepted educational settings. . West Virginia University. Office of Research Integrity & Compliance. Human Research Protections Program. Human Subjects Research. Any . Human Subjects Research conducted by or under the auspices of any WVU faculty, student or staff must be reviewed by the WVU IRB. . HOSPITALS AND OTHER PROPERTY. Presented by:. Mark e. Giaquinta. Sarah . l.. . schreiber. EXEMPTIONS GENERALLY. EXEMPTIONS GENERALLY. What?. Reduce tax obligation; or. Eliminate obligation to pay tax.. Objectives. Define research and human subjects research.. Show the "gray area" between research and practice.. Describe the distinction between a medical education initiative and a medical education research initiative.. S. Percy Ivy, MD. Associate Chief, Senior Investigator. Investigational Drug Branch, National Cancer Institute. ivyp@ctep.nci.nih.gov. . National Cancer Institute. . National Cancer Institute. MBA. Director, Investigator Support & Integration Services, OCTRI. January 26, 2011. Journal of Clinical Research Best Practices. Vol. . 7, No. 1, January 2011 . “. Can You Handle the Truth. S. Percy Ivy, MD. Associate Chief, Senior Investigator. Investigational Drug Branch, National Cancer Institute. ivyp@ctep.nci.nih.gov. . National Cancer Institute. . National Cancer Institute. in Research. http://orip.syr.edu/humanresearch.html. Office . of Research Integrity and Protections . (. ORIP) . . What Is the Institutional . Review Board and what is it’s role?. The IRB must be comprised of at least 5 members from relevant academic disciplines and include at least one non-affiliated community member.. New Faculty Onboarding. Gretchen McMasters, MBA, CHRC, CIP, CIM, LSSBB. WVU OHRP Director. Topics . IRB responsibility and authority. “FLEX” application . IRB submission guidance. What is an IRB? . IRBNet at Lehman. Tara M. Prairie . Director of Responsible Research Practices. Lehman College. Overview. Types of Review. Training . www.citiprogram.org. IRBNet . www.irbnet.org. Guiding Student Research.