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PAREXEL Experts to Present Leading Insights at Drug Information Association Annual Clinical Forum
Date:10/19/2009

BOSTON, Oct. 19 /PRNewswire-FirstCall/ -- Experts from PAREXEL International Corporation (Nasdaq: PRXL), a leading global biopharmaceutical services provider, will address important industry issues at the Drug Information Association (DIA) 3rd Annual Clinical Forum, being held from October 19 - 21, 2009 in Nice, France. A number of PAREXEL's thought leaders will present on topics ranging from pharmacovigilance reporting to centralized monitoring for late phase trials. Presentations from PAREXEL and its subsidiary, Perceptive Informatics, a leading eClinical solutions provider, will also discuss best practices for the integration of technology in post-marketing studies as well as data checks in Electronic Patient-Reported Outcomes (ePRO) based studies.

Attendees at the meeting will be able to learn more about capabilities related to these topics by visiting the PAREXEL Booth #16 or Perceptive Informatics Booth #13 in the exhibit hall. The DIA Annual Clinical Forum program features the following sessions:

Monday, October 19

  • The European Annual Safety Report: A case study in best practice for outsourcing pharmacovigilance writing to a global CRO - Julia Cooper, PhD, Senior Director, Worldwide Head of Medical Writing Services, PAREXEL (4:00 p.m. - 5:30 p.m.)
  • Simple Data Checks to Check for Fraud Data: A case study on the process of fraud detection in ePRO studies - Hannah Jane O'Gorman, Associate Director, ePRO Operations, Perceptive Informatics (4:30 p.m. - 5:30 p.m.)

Wednesday, October 21

  • Centralized Monitoring in Late Phase Studies: Shifting the paradigm - Ramita Tandon, Senior Director, Global Portfolio Management, Peri-Approval Services, PAREXEL (9:00 a.m. - 10:30 a.m.)
  • The ICF: A balancing act - James Wolfe,
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SOURCE PAREXEL International Corporation
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