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DIA Safety Conference To Explore Solutions To Challenges Facing Pharmaocovigilance And Risk Management Strategies
Date:11/19/2009

IOMS) on Drug Safety Update Reports (DSURs) in premarketing clinical trial safety
  • New approaches to risk management, risk communication, labeling and packaging to optimize medical product benefit while minimizing preventable harm

  • “Robust drug safety systems and processes and thorough ongoing safety surveillance are more critical than ever in the development and evaluation of the safe use of marketed medicinal products,” says,
    Program Committee Member Mariette Boerstoel-Streefland, MD, MBA, MS(epi), Executive Director, Pharmacovigilance/Risk Management, Forest Research Institute, Forest Laboratories Inc. “This conference will provide safety professionals with the latest pharmacovigilance regulatory advances and state-of-the-art risk management strategies."

    Pre-conference tutorials on January 9 will focus on:

     
    • Signal Detection, Case Assessment and Data Mining in Pharmacovigilance: Current State of the Art
    • Periodic Safety Update Reports (PSUR): A Guide to the Construction and Analysis of PSURs, ASRs, and DSURs
    • Applied Epidemiology Techniques for Pharmacovigilance Risk Management
    • Applying MedDRA® in Clinical Safety, Pharmacovigilance and Labeling
    • Pharmacovigilance and Risk Management Planning

    Register for the 9th Annual Conference
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    Source: PRWeb
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