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DIA 3rd Annual Clinical Trial Disclosure Workshop Offers Strategies for Creating Effective Registries and Results Databanks
Date:8/20/2009

The Drug Information Association (DIA) will host its 3rd Annual Clinical Trial Disclosure Workshop (October 6-8, 2009; National Harbor, MD).

Horsham, PA, USA (Vocus) August 20, 2009 -- The Drug Information Association (DIA) will host its 3rd Annual Clinical Trial Disclosure Workshop (October 6-8, 2009; National Harbor, MD).

This three-day workshop will feature interactive discussions with government, biopharmaceutical, medical device, and data standards experts on how to ensure compliance and improve efficiency in clinical trial disclosure.

FEATURED TOPICS

 
  • Global Requirements, Laws, Regulations and Business Cases
  • Defining the Clinical Trial Disclosure Role within a Company
  • Available Tools, Resources, Organizations
  • Impact of External Stakeholders, Company Policies, and Advanced Technologies on
  • Disclosure Processes
  • Key Milestones for Managing Compliance
  • Quality Checks
"Evolving clinical trial registration and results disclosure requirements are significantly increasing the workload of clinical operations and medical affairs departments," says Program Co-chair Tracy Beck, PhD, Associate Global Medical Business Office Consultant;
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Source: PRWeb
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DIA 3rd Annual Clinical Trial Disclosure Workshop Offers Strategies for Creating Effective Registries and Results Databanks 
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