Unique Device Identification Jay Crowley Senior Advisor for Patient Safety Food and Drug Administration [email protected] 301-980-1936.
ClinicalTrials.gov Why Does it Affect Me? Should I Be Concerned? Presenter Name and contact Info.
ClinicalTrials.gov Why Does it Affect Me? Should I Be Concerned? Adapted from the work of the Clinical and Translational Science.
1 Introduction Fred D. Lublin, MD Saunders Family Professor of Neurology Director, The Corinne Goldsmith Dickinson Center for Multiple Sclerosis Mount.
Lecture one, units 1 2 pharm
10 Tips for Developing and Implementing a Unique Device Identification (UDI) Program
2008 Health Care Forecast Conference Prospects for Federal Health Legislation Irvine, California February 21, 2008 Dean A. Rosen Mehlman Vogel Castagnetti,
NATIONAL CLINICAL TRIAL (NCT) NUMBER Clinical Trials Management Office December 17, 2014.
Unique Device Identification (UDI) – Enabling the Transformation of Medical Device Safety
Medical Device Provisions of the FDA Amendments Act of 2007
Unique Device Identification (UDI) – Transforming the Global Medical Device Landscape