SoCRA Review: Investigator Roles and Responsibilities in Clinical Research John Naim, PhD Director Clinical Trials Research Unit West Virginia University.
Ethics in Experimental Research Showing concern for the welfare of human subjects.
RESEARCH COMPLIANCE Due Diligence and Institutional Review Boards - How Much Oversight is Enough? Janet K. Himmelreich Managing Director ZA Consulting,
Research Compliance: Regulatory Implications for Researchers.
Responsible Conduct of Research Fall-1, 2013 Delia Y. Wolf, MD, JD, MSCI Assistant Dean, Regulatory Affairs and Research Compliance Harvard School of Public.
University of Miami. HSRO Mission Protecting the safety, rights, and welfare of human research participants through: Collaboration and Regulatory Compliance.
GCP 101 or Why we do What we do the Way we do it Elaine Dempsey.
1 IRB Presentation University of Central Florida Office of Research & Commercialization 407-823-2901 or fax 407-823-3299 .
AAHRPP Association for the Accreditation of Human Research Protection Programs Thanks to: Lisa Demanuel, Program Specialist Brain Rehabilitation Research.
Fourth Annual Medical Research Summit Preconference II – Workshop on FDA Enforcement, Fraud and Abuse, OIG Guidance and Other Compliance Issues in R&D.
Human Subjects Protection
Institutional Review Board