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

The Drug Information Association (DIA) will host Safety is Global: Contemporary Pharmacovigilance and Medical Product Risk Management Strategies (December 10-12; Marina Square, Singapore).

Horsham, PA (Vocus) October 28, 2008 -- The field of medical product safety continues to grow in complexity, with both clinical trial safety and post-marketing pharmacovigilance becoming ever more critical in the development and marketed use of medical products. In response, the Drug Information Association (DIA) will host Safety is Global: Contemporary Pharmacovigilance and Medical Product Risk Management Strategies (December 10-12; Marina Square, Singapore).

This unique three-day conference will explore the latest safety-related regulatory initiatives, how to optimally utilize epidemiological, clinical pharmacological and other techniques, state-of-the-art risk management strategies, and how all of this can be pulled together to create a "system." Featured topics will include:

  • Latest international regulatory developments
  • Generating and assessing critical safety data during development
  • Compliance with clinical safety and post-marketing pharmacovigilance regulatory requirements in an evolving global environment
  • Relationship between compliance and quality in safety-related processes and procedures
  • Recent multinational initiatives under the Inte
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DIA Conference to Explore Global Pharmacovigilance and Risk Management Strategies and Regultory Frameworks
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