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A new dawn for regulation of medical technologies in the UK post-Brexit? From European directives to the proposed stand-alone regulatory regime for the future

Last month the Medicines and Healthcare products Regulatory Agency launched a public consultation on the future of medical device regulation in the UK.

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FDA Draft Guidance Would Restrict Marketing of Research Use Only and Investigational Use Only In Vitro Diagnostic Products

Practices: Life Sciences Industries: Biotechnology & Pharmaceuticals

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