| Description |
Follow-up to the Successful 2007 Clinical Trial Disclosure Workshop: Learning the Landscape and Reading the Roadmap.
Gain expert insight from government, pharmaceutical, biotechnology, and medical device professionals on how to ensure compliance with clinical trial disclosure laws and regulations, the Clinical Trials.gov registry, and results database.
FEATURED TOPICS
•NIH Registry And Results Database
•Challenges with Journal Requirements and Legislation
•Academic and Independent Investigator Compliance
•EMEA Systems, Requirements and Developments
•Perspectives and Points of View
•Registries and Results Databases Requirements in the International Community
•Company Processes to Handle Disclosure Activities
•Legislative Actions and Reactions.
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