PPT-Getting Started with Human Subjects Research

CITI and eIRB access Educational Requirements The Collaborative Institutional Training Initiative CITI is an online educational course about research ethics WFU subscribes to CITI through the University of Miami. Or, . Why Bad . Cases Make Tough Laws!. Objectives: By the end of this lecture..... 1. You will have . stopped . wondering why . there . are so many conflicting results out there.. 2. You will have stopped wondering why there are so many hoops to jump through in order to do research.. Wilna. . Venter, M.A., M.Ed.. Cluster Manager: Strategic Support. University of Cape Town Research Office. Content. Historical . background . Definition . of research . integrity and ethics. Responsible conduct of . uversity.com/reseah GETTING STARTED WITH STUDENT AMBASSADORS Introduction High school students want authenticity. When marketing your institution to prospective students, clear is the new clever. & 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. Julie M. Aultman, Ph.D.. Chair, Institutional Review Board. Associate Professor, Family and Community Medicine. Northeast Ohio Medical University. Important Questions. What is research?. What is human subjects research?. NIH . Regional Seminar. Yvonne Lau, . MBBS, MBHL, . PhD. Director, Division . of Education and . Development (DED). Office for Human Research Protections (OHRP). Department of Health and Human Services (HHS). Basic hhs and nih requirements. Yvonne lau – Office of human research protections. Ann hardy – Nih Office of Extramural research. Dawn Corbett – NIH Office of extramural research. May 2017. Describe the role of the Office for Human Research Protections (OHRP) and the federal regulations on human research protections;. Steven J. Squires, MEd, MA, PhD. IACRN. Wednesday, September 16, 2015. Background and Disclosure. System Director of Ethics for Mercy Health. Ph.D. Health Care Ethics, M.A. in Biomedical Ethics and Health Care Policy, M.Ed. in College Student Personnel – Administration.. September 4, 2015. IRB Basics. What is an IRB?. I. nstitutional . R. eview . B. oard (responsible to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated) . Office of Research Administration. Important to Note. These slides are not intended to replace the required CITI training on a long-term basis. Rather, they are being provided to researchers focused on COVID-19 research . Kodu CurriculumGetting Started withKeyboardand Mouse PC Requirements Kodu requires a Windows Operating SystemDirectX9 graphicsShader Model 2.0 or greater. How to Check Your DirectX VersionFor Windows Subjects. Freda E. Yoder. Division of Education and Development. Office for Human Research Protections (OHRP). Department of Health and Human Services (HHS). Ann M Hardy, Dr.P.H.. NIH Extramural Human Research Protection Officer. HHS Office for Human Research Protections (. OHRP. ). Division of Education and Development (. DED. ). Disclaimer. The opinions expressed are those of the presenter and do not necessarily reflect the policy of the U.S. Department of Health and Human Services.. Chris . Sylvester, M.A.. Senior Grant Administrator (AO). Grants and Contracts. 617-414-2879. christopher.sylvester@bmc.org. A research study in which one or more human subjects are prospectively assigned .