Learn How to Remove Roadblocks and Navigate the Public Registration Process of Clinical Trials
WHAT YOU WILL LEARN This unique webinar will provide practical advice and tips for complying with worldwide regulations and recommendations for public registration of clinical trials at study inception/initiation.
Organized by:
Drug Information Association
Invited Speakers:
1)BARBARA GODLEW,, RN Associate Director, Public Coordination and Transparency Compliance Exploratory Development Novartis Pharmaceuticals Corp.
2)PAMELA ROSE,, RN,, FNP,, ASQ--CMQOE Director, Clinical Trial Information Registries R&D TAP Pharmaceutical Products, Inc.
3)PEGGY DOLIIN--BRUNEL, MSc Transparency Initiatives Unit Leader Global Medical Affairs – Clinical Operations Sanofi-Aventis Group