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PAREXEL Experts to Present Leading Insights at Drug Information Association 21st Annual Euromeeting
Date:3/5/2009

BOSTON, March 5 /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) 21st Annual EuroMeeting, being held from March 23 - 25, 2009 in Berlin, Germany. A number of PAREXEL's thought leaders will present on topics ranging from global biosimilar development programs, medical device and combination products, and clinical process validation to early stage compound selection and pharmacovigilance reporting. PAREXEL experts will also discuss best practices for managing risk in supplier selection, integrating eClinical technologies, and conducting clinical trials multi-nationally and in emerging regions.

A complimentary European Union (EU) Pediatric Investigation Plan (PIP) Advisory from PAREXEL Consulting, with an update and guidance on how biopharmaceutical companies should address the new PIP requirements, will be provided at PAREXEL's Booth #1522. PAREXEL experts will also be available at the booth to hold exclusive executive briefings with companies on emerging EMEA/FDA cooperation regarding new drug reviews, strategic regulatory partnering, follow-on biologics, and portfolio analysis among other key topics.

Attendees to PAREXEL's booth will be able to view a demonstration of the DataLabs(R) Electronic Data Capture (EDC) and Clinical Data Management System (CDMS) from Perceptive Informatics, which is focused on improving the efficiency and data quality of clinical studies. The system incorporates the advantages and flexibility of hybrid technology, unifying paper data entry and EDC into a single clinical data management platform.

The DIA EuroMeeting program features the following sessions, which will be presented or chaired by PAREXEL experts
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