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PharmQuest develops a suite of innovative products and solutions enabling pharmaceutical and biotechnology companies to maximize their R&D investment and facilitate electronic submissions to regulatory agencies.

PharmQuest's products are developed using standards-based, open-architecture software modules that can be fully integrated to enhance project, information and knowledge management company-wide. PharmQuest Corporation is a leading provider of SEND (Standard for Exchange of Nonclinical Data) enabling technology.

The US Food and Drug Administration (FDA) and PharmQuest entered into a CRADA (Co-operative Research and Development Agreement) to develop standard data evaluation and review tools for electronic submission of animal safety data. Working primarily with FDA reviewers and industry experts, we developed ToxQuest for drug safety and toxicology data. This solution is used by leading pharmaceutical companies and Contract Research Organizations (CROs).

Contact us today to learn how you can maximize your SEND opportunities. We look forward to working with you.

  LATEST NEWS AND EVENTS
Charles River Laboratories Preclinical Services Montreal Chooses Instem-PharmQuest submit™ Solution For FDA's SEND Standard
PharmQuest to present at ODM and SDTM Seminars, July 26-27, 2005, San Francisco.
PharmQuest presents at IIC 2005, May 23-25, 2005, Edinburgh, Scotland.
 



PharmQuest is now a part of PointCross.



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