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DIA Conference to Present Latest Strategies in Clinical Trial Disclosure Compliance
Date:9/17/2008

Experts from government, the pharmaceutical and biotech industries, and medical device companies will discuss best practices to ensure compliance with clinical trial disclosure laws and regulations, the Clinical Trials.gov registry, and results database during the Drug Information Association's (DIA's) Current Advancements in Clinical Trial Disclosure: The Changing Tide (October 15-16; Chicago, IL).

Horsham, PA (PRWEB) September 17, 2008 -- Experts from government, the pharmaceutical and biotech industries, and medical device companies will discuss best practices to ensure compliance with clinical trial disclosure laws and regulations, the Clinical Trials.gov registry, and results database during the Drug Information Association's (DIA's) http://www.diahome.org/DIAHOME/Education/FindEducationalOffering.aspx?productID=17203&eventType=Meeting [Current Advancements in Clinical Trial Disclosure: The Changing Tide] (October 15-16; Chicago, IL).

This follow-up to the successful 2007 Clinical Trial Disclosure Workshop will feature myriad topics, including:

  • Challenges with journal requirements and legislation
  • Academic and independent investigator compliance
  • EMEA systems, requirements and developments
  • Registries and results database requirements in the international community
  • Company processes to handle disclosure activities
  • Legislative actions and reactions
About the http://www.diahome.org/DIAHome/ [Drug Information Association (DIA)]
DIA serves more than 30,000 professionals in the biotechnology, pharmaceutical an
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