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PAREXEL Experts To Address Best-Practice Strategic Partnership Models To Increase Operating Efficiency, Development Effectiveness at Partnerships in Clinical Trials
Date:3/17/2011

ogram also features the following sessions by PAREXEL experts, which focus on achieving high levels of quality in clinical development to optimize outcomes:

  • eClinical Technology Track, March 31, 11:45 a.m.:  Achieve Closer Integration of Clinical Operations Data (EDC, IVRS, CTMS) to Improve Quality and Optimize Clinical Outcomes—John Humphreys, Product Director, CTMS

  • Regulatory Compliance & Quality Oversight Track, April 1, 11:00 a.m.:  Implement a Comprehensive Clinical Trial Drug Safety Program and Improve Quality from Clinical Development to Post-Approval—Ramita Tandon, Senior Portfolio Director, Late Phase

  • For more information about PAREXEL visit www.PAREXEL.com or Booth #707 during the conference. Information about Partnerships in Clinical Trials can be found at www.clinicaltrialpartnerships.com.

    About PAREXEL InternationalPAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement.  Perceptive Informatics, Inc., a subsidiary of PAREXEL, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process.  Headquartered near Boston, Massachusetts, PAREXEL operates in 71 locations throughout 52 countries around the world, and has approximately 10,380 employees. For more information about PAREXEL Internati
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