ec/irb
Assurance
Annual Report 2009
2009 Managing COI in Research
Safety Workshop: Part I Clinical Trial Safety and Safety Monitoring August 18, 2010 Albert Yoyin, M.D. DAIDS Regulatory Support Center (RSC) August 18,
AACSB INTERNATIONAL Global Accreditation-Getting Started James M. Daley Rockhurst University Karel Soudan University of Antwerp Joseph M. Phillips Albers.
Whats Going On? Five Year Reviews and Assessment: Sharing Experiences so Far Ruth Guzley, Mike Ward and Bill Loker, AURA.
1 HSPP Overview – IRB Members (Boards 1, 2, 3) University of Illinois at Chicago Office for the Protection of Research Subjects Charles Hoehne, Education.
The Institutional Review Board M. Jeffery Mador, M.D. Chair-Buffalo VAMC IRB Associate Professor of Medicine.
An FDA Audit: What the Investigator and Sponsor Need to Know zJoseph P. Salewski, Chief zBioresearch Monitoring Branch zCenter for Biologics Evaluation.
ICH Harmonised Tripartite Guideline for Good Clinical Practice Part I (Principles, IRB/IEC, Investigator, Sponsor) Josip Arlica, MD Altiora Training Program.
IRB Basics Presenter: Janelle Greening, M.B.A., C.I.P. Compliance Officer Revised: April 2012 1.
