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Advena Ltd
Consultants to the medical device industry with over 25 years experience in International regulatory affairs. Specialising in creating and maintaining quality management systems and the writing of technical files as well as working with manufacturers from design through to regulatory approval. Established Authorised Representatives for non-European manufacturers.
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Events
The Collaborative Healthcare Leadership Programme |
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20th February 2012 Faced with diminishing resource and budget, Leaders within the NHS are having... |
Pre-clinical Evaluation in Drug Development |
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7th March 2012 The aim of this unique short course is to provide a detailed insight into the... |
Clinical Evaluation of Medical Technology |
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13th March 2012 The course is designed to help regulatory professionals understand the fundam... |
Management of Regulatory Affairs & its Contribution to the Medical Technology Lifecycle |
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12th June 2012 The course is designed to provide students with an understanding of the skill... |
Sponsors
Cranfield’s qualification – in collaboration with The Organisation for Professionals in Regulatory Affairs (TOPRA) – combines TOPRA’s long-standing experience and expertise with Cranfield’s strong academic reputation and its links to industry