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Referans
Differences in OHRP, FDA and ICH Regulations/Guidelines Monika Haugstetter, MHA, MSN, RN Human Subject Protection Office (HSPO) and Institutional Review.
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HUMAN SUBJECTS PROTECTION AND DATA PRIVACY IN PBRN RESEARCH Barbara Daly, PhD, RN, FAAN Professor, CWRU Director, Clinical Ethics, Univ. Hosp. of Cleveland.
Disclosure I, Peter T. Katzmarzyk, PhD, FACSM, have no relationships with commercial interests to disclose. A commercial interest is any entity producing,
Tool: Training Presentation: Clinical Research Responsibilities for NIDCR-Funded Investigators Purpose: To provide an overview of the key roles and responsibilities.
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Ethics in Violence Research with Vulnerable Populations April 24, 2006 Sponsored by: Interdisciplinary Center for Research on Violence Criminal Justice.
Human Subjects Protection: Creation and Maintenance of an IRB Regulatory Requirements & Recommendations 45 CFR part 46 Freda E. Yoder Office for Human.
