MEETINGS - Validation in the Medical Device Industry (UK) June 1998:
This article was originally published in Clinica
Management Forum will hold a meeting on Validation in the Medical Device Industry in London on June 29. It will provide an introduction to validation - the master plan and its associated documentation, the procedures involved, the protocols and the reports. Discussion topics will also include the new FDA software guidelines and its basic concepts, and regulatory requirements for validation by the European system and the FDA. For more details contact Management Forum in the UK. Tel: +44 1483 570 099. Fax: +44 1483 536 424.
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