Multi Track Session
|Drug Development: Ethics and Public Confidence is a Must
University of Maryland School of Medicine USA
Dr. Shamoo is the Founder & Editor – Chief (Since 1988) of the journal, Accountability in Research and a member of several boards among them the
editorial board of the Drug Information Journal (2005-present) and advisory board of 2005-2007 of: Public Library of Science, Clinical Trials
(PLos Clinical Trials).
|Adil Shamoo, Ph.D|
|Confronting the Compliance Myth: How can we Really Protect Human Subject?
Department of Anesthesia and Critical Care, USA
Dr. Koski is currently Senior Scientist at the Institute for Health Policy at the Masschusetts, Harvard Medical School.
Dr. Koski chairs the Ethics Advisory board of the National Heart Lung and Blood Institute’s renowned Framingham Heart Study and the chair
person for the advisory board of the Strategic Initiative for Developing Capacity for Ethical Review based at the WHO.
|Greg Koski, Ph.D, MD|
|Ethical Decision Making in Clinical Research Management…Listening to your Moral Imperative
Vice President of Human Research Technology Inc. USA
Mr. Koscin serves as the Lead Forum Chair for the Association of Clinical Research Professional (ACRP) special interest forums, an active member of
the ACRP Marketing & Communication Committee and the Lead Instructor for the certificate course Pathways in Clinical Research.
|Mark Koscin, M.T., CCRA, ACRP|
|Exploring Ethical Issues Beyond Good Clinical (Research) Practice
Former Vice President
Mr. Tom Merchant is an attorney and the former Vice President of R&D Legal Risk Management at GlaxoSmithKline Pharmaceutical in Suburban
Philadelphia. He recently led a US/UK based group responsible for auditing worldwide R&D risk which have a significant legal component or pose
significant risk reputation.
|Thomas E. Merchant, ESQ|