Monitoring Clinical Drug Studies: Advanced

Published: 25-Aug-2011

18 - 19 October 2011
Course
Philadelphia, PA, US

Topics include site management, developing or identifying and modifying tools for effective monitoring and co-monitoring assessments, challenges in our global environment, and successful time management. Discussion will include how sponsors/CROs interpret and implement various aspects of clinical trials such as adverse event reporting and managing non-compliant or underperforming sites. This course will also run in San Diego, CA on 1 - 2 December

Organiser: Barnett International

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