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FDA Inspects Hovione's Technology Transfer Center in New Jersey
Date:10/29/2007

GMP facility is designed to prepare small quantity NCE's to support customer's pre-clinical and early-phase clinical development, demonstrating the customer's processes locally before transferring them to Hovione's full scale manufacturing plants, in Europe and Asia.

Hovione is an international group specializing in the development and compliant production of active pharmaceutical ingredients (APIs), serving exclusively the pharmaceutical industry. With a 48-year track record in process development, quality standard and advanced particle design technologies, Hovione offers APIs for all drug delivery systems, from oral to injectable and from inhalation to topical applications. With FDA inspected plants in Europe, Far East and New Jersey, Hovione is committed to the highest levels of service and quality. Specializing in complex chemistry, Hovione offers services related to the development and manufacture of either a new chemical entity (NCE) for an exclusive contract manufacturing partner or an existing API for an off-patent product.

For further information about Hovione, please visit the Hovione site at http://www.hovione.com

Contacts:

Corporate Communications,

Isabel Pina,

+351-21-982-9362,

e-mail: hello@hovione.com


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