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DIA Conference to Explore Global Pharmacovigilance and Risk Management Strategies and Regultory Frameworks
Date:10/28/2008

rnational Conference on Harmonization (ICH) and Council for International Organizations of Medical Sciences (CIOMS)
  • New approaches in risk management, risk communication, labeling, and packaging to optimize medical product benefit while minimizing preventable harm
  • Patient safety
  • "Safety professionals from countries and regions that do not participate in ICH will learn about the latest pharmacovigilance regulatory advances, how to optimize epidemiological and clinical pharmacological techniques in both clinical safety and post-marketing, and state-of-the-art risk management strategies," says Program Chair Stephen A. Goldman, MD, FAPM, DFAPA, Managing Member, Stephen A. Goldman Consulting Services, LLC. "In addition, there will be updates on regulatory frameworks for pharmacovigilance in the US, EU, Japan, Australia, New Zealand, Singapore, Thailand, India and China in an effort to foster greater cooperation and collaboration for global patient safety."

    About the Drug Information Association (DIA)
    DIA serves more than 30,000 professionals in the biotechnology, pharmaceutical and regulatory industries worldwide. Through its domestic and international meetings, training courses, workshops and webinars, DIA provides a neutral global forum for the exchange of information critical to the advancement of the drug discovery and lifecycle management processes. Headquartered in Horsham, PA (USA), and with offices in Basel, Switzerland, Tokyo, Japan, Mumbai, India, and Beijing, China, the Association is led by its volunteer-based Board of Directors and executive management team. For more information, visit www.diahome.org or call 215-442-6100.

    Contact: Joe Krasowski
    +1-215-293-5812
    Joe.Krasowski @ diahome.org

    ###

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