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PAREXEL to Address New Regulatory Guidelines and Data Standards at DIA EuroMeeting
Date:3/22/2012

challenges of cell-based therapeutics, the new regulation 1394/2007NRalf Hess, PhD, MSc, Principal Consultant (11:00)
  • Session 0807:  Quality Requirements for Clinical TrialsNSusanne Franke, MSc, Senior Manager, Clinical Logistics (14:00)
  • Session 0808:  Metal Catalysts and Others: Analytical and Safety Assessment Demands for Pharmaceuticals Emerging from Regulatory GuidelinesÑAnders Neil, PhD, Principal Consultant (16:00)
  • For more information about PAREXEL visit www.PAREXEL.com or Stands 326 and 328 during the meeting. Information about the DIA EuroMeeting can be found at http://www.diahome.org.

    About PAREXEL International
    PAREXEL International Corporation is a leading global biopharmaceutical 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 11,300 employees. For more information about PAREXEL International visit www.PAREXEL.com.

    This release contains "forward-looking" statements regarding future results and events, including, without limitation, statements regarding expected fi
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