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Biotech / Medical : Xenova (XNVA)
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To: nigel bates who wrote (62)6/21/2004 4:10:07 AM
From: tuck   of 173
 
Dunno, I don't remember or never knew how big the market is supposed to be. Meanwhile, in the every little bit helps department . . .

>>SLOUGH, U.K., June 21, 2004 (PRIMEZONE) -- Xenova Group plc (London:XEN.L - News) (NasdaqNM:XNVA - News) announced today that it has received a Manufacturer's Authorisation -- Investigational Medicinal Products from the Medicines and Healthcare products Regulatory Agency (MHRA) for its clinical trials manufacturing facility (CTMF) in Cambridge.

This authorisation allows Xenova to manufacture and release investigational medicinal products (IMPs) in compliance with the new Clinical Trials Directive which came into force in May of this year. The authorisation will apply to Xenova's own products and those manufactured at Xenova under contract for clients. The licence was awarded after the MHRA inspected the company's premises and confirmed compliance with the EU Good Manufacturing Practices (GMP), which Xenova received in September 2003.

Mike Johnston, Director of Manufacturing and Process Development at Xenova, said, ``This authorisation confirms that we are compliant with manufacturing standards that are required under the new clinical trials directive and through the utilisation of excess capacity we can assist other companies in the production of GMP products as well as ensure all Xenova products manufactured at the CTMF are of the highest clinical standard.''<<

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Cheers, Tuck
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