The Safety Continuum in the Medical Product Life Cycle

September 22 - 24, 2010 Baltimore, MD

During this three-day conference, experts offer strategies to overcome critical drug safety challenges faced through-out a product’s life cycle from premarketing clinical trials all the way to postmarketing safety surveillance/vigilance, and risk management.  Participants learn about current regulatory national and international standards, state-of-the art methods and techniques in premarketing testing and evaluation, quality safety-related compliance and procedures, effective signal detection and assessment, adverse event reporting, and the latest risk management approaches in the US and abroad.

For more information: www.iirusa.com/medicalproductsafety/conference.xml

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