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CHI’S POST-APPROVAL DRUG SAFETY STRATEGIES

Type Conference
Date November 12, 2008 to
November 14, 2008
Venue Ritz-Carlton, Pentagon City

Arlington, VA
US
Chemistry Specialties
  • medicinal and pharmaceutical chemistry
Chemistry Techniques
  • other
Contact CHI Representative
Cambridge Healthtech Institute
250 First Ave
Needham, MA 02494
US
781 972 5400
781 972 5425
chI@healthtech.com
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by Robert Black last modified 06-18-08 06:31 AM

Improving products’ effective clinical safety will increase the industry’s fundamental value proposition to patients, healthcare providers, payors and regulators. The program will focus on pharmacovigilance program implementation and specific strategies and approaches to creating true value from a peri- and post-approval drug safety program. Drug safety programs and monitoring and the approach of this conference are not to look at safety in the silos of early-phase safety or post-approval safety but to view safety holistically, across the lifecycle, especially at the transition from approval to broader use in the marketplace. www.healthtech.com

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