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Legal Manufacturers of In Vitro Diagnostic products need to be aware of the scope and implications of the new European In Vitro Diagnostics Regulations 2017/746. Organisations must be realistic and prepared. Not only for the impact of changes in the short-term, but for the long-term implications to the development and maintenance of diagnostic products in […] |
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Wednesday 16th October 2019 Hill Dickinson, Broadgate Tower, 20 Primrose Street, London EC2A 2EW, 10:30 – 16:00 SEHTA members fee - £250 + VAT per delegate SEHTA non-members fee - £300 + VAT per delegate Why attend Clinical strategy, evidence and evaluation are central to product approval and market access. Through clinical data a company […] |
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