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PRA International Experts Present at the 45th Annual DIA Meeting
Date:6/17/2009

RALEIGH, N.C., June 17 /PRNewswire/ -- PRA International, a leading Clinical Research Organization, announces it will present and exhibit at the 45th Annual Drug Information Association (DIA) meeting June 21 - 25 in San Diego, California. On June 21, Dr. Paul Starkey, PRA's Executive Director of Medical Affairs will make a presentation entitled "Obtaining Good Quality Data from Investigative Sites."

In addition, Dr. Starkey and other PRA medical, regulatory and operational experts will host Roundtable Sessions at PRA's booth # 811 on June 22nd and 23rd. The following topics will be addressed in one-hour interactive sessions:

  • Protocols, Waivers and Serious Breaches
  • Meeting The Requirements of Blending REMS Science & Operational Execution
  • Strategic Alliances to Ensure Product Development Success
  • Compassionate Use/Expanded Access Programs
  • Real-time Access to Data in Phase I

PRA will also have representatives from the following groups available to answer questions about PRA's capabilities in executing Phase I through Phase IV studies: Early Development Services, Medical Affairs, Data Management, Project Management, Clinical Operations, Regulatory, Late Phase Services, Executive Management and Business Development.

About PRA International

PRA International conducts clinical trials in more than 65 countries across 6 continents and provides services through all phases of clinical development. PRA performs studies in all therapeutic areas, with specialization in Oncology, Neurosciences, Respiratory/Allergy, Cardiovascular and Infectious Diseases. PRA has supported over 2,100 clinical trials through its 35 global offices.

PRA's therapeutic expertise, global reach and project experience, combined with extensive local kn
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SOURCE PRA International
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