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Thomson Reuters Introduces a New Solution to Boost Competitive Advantage in China's Generics and API Market
Date:6/23/2008

ttp://scientific.thomsonreuters.com .

About Thomson Reuters

Thomson Reuters is the world's leading source of intelligent information for businesses and professionals. We combine industry expertise with innovative technology to deliver critical information to leading decision makers in the financial, legal, tax and accounting, scientific, healthcare and media markets, powered by the world's most trusted news organization. With headquarters in New York and major operations in London and Eagan, Minnesota, Thomson Reuters employs more than 50,000 people in 93 countries. For more information, go to http://thomsonreuters.com .

Notes to Editor:

(1) CPhI China 2008 is held at Shanghai New International Expo Centre from 24-26 June and is the leading exhibition on pharmaceutical ingredients and allied industries http://www.cphi-china.com

Mr. David Harding, Newport Specialist, Scientific business of Thomson Reuters, will be presenting during CPhI on 25 June 2008 at 2:30PM at E5 Exhibition Hall.

(2) US Drug Master File (DMF): A confidential document covering a specific manufacturing facility, process or article used in the manufacture, processing, packaging or storing of a bulk drug (API), which is covered in an ANDA. DMFs are never approved or disapproved by the FDA, but are kept on file and only reviewed when a manufacturer files an ANDA (Abbreviated New Drug Application) or an NDA referencing the DMF.

For more information, please contact:

Pamela Lim

Manager, PR & Communications

Scientific

Tel: +65-6411-6737

Email: pamela.lim@thomsonreuters.com


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SOURCE Thomson Reuters
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