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PAREXEL Experts to Address Key Industry Topics at the Drug Information Association 44th Annual Meeting
Date:6/16/2008

Understanding the Regulation of Advanced Therapy Medicinal Products in

Europe, Introduction to the New Regulations on Advanced Therapy

Medicinal Products -- Session Chair and Speaker: Ralf Dieter Hess, PhD,

MSc, Principal Consultant, PAREXEL Consulting (1:30 p.m. -- 3:00 p.m.)

-- Outsourcing in China: Opportunities and Challenges Decision Models and

Case Study -- Session Chair and Speaker: Simon Wang, MBA, MSc, Manager,

PAREXEL APEX International (1:30 p.m. -- 3:00 p.m.)

-- Nanotechnology Task Force: Regulating Nanotechnology Products, FDA's

Exploratory IND Guidance: Transitioning Nanotechnology Drugs/Biologics

-- Session Chair and Speaker: George Q. Mills, MD, Vice President,

Medical Imaging Consulting, Perceptive Informatics

(3:30 p.m. -- 5:00 p.m.)

-- Leveraging Technology to Build an IT Infrastructure for Global Clinical

Trials, Scaling EDC Solutions to Meet the Needs of Large-Scale Global

Trials -- Ian Sparks, Consultant, Worldwide EDC Solutions Group,

Clinical Research Services, PAREXEL (3:30 p.m. -- 5:00 p.m.)

The DIA Annual Meeting attracts approximately 8,000 attendees, bringing together professionals from the biopharmaceutical and related industries. This year's meeting will feature nearly 360 sessions across 26 tracks and will cover several hot topics including adaptive trials and methods, patient recruitment and retention, multinational clinical trials, clinical and regulatory considerations for personalized medicine, and various biotechnology related topics.

For more information about PAREXEL visit http://www.PAREXEL.com or Booth #803 at the DIA Annual Meeting.

About PAREXEL International

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medica
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