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PHARMACEUTICAL
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GLOBAL MANUFACTURING
SITE TRANSFER

REGULATORY AND QUALITY CONSIDERATIONS

Conference Date: 28-29 Jan 2009
Conference Ref: A1-6109
Fee: £1280 + VAT
Venue: Harrington Hall Hotel, London

This seminar will provide you with an overview of the regulatory, quality and project management considerations required for the efficient and effective transfer of both API and drug products between manufacturing sites, as well as the co-ordination of these activities with name changes, packaging and formulation rationalisation.