An update on what’s happening in medical regulations by Alison Dennis of Taylor Wessing.

Fewer than 50% of the Medical or In Vitro Diagnostic equipment which will need to be certified to meet the new MDR and IVDR, have achieved certification, and time is rapidly running out. Over half the applications for certification made so far under the MDR have been rejected which also bodes ill for the chances of IVD applicants for whom this is an entirely new process.

Things are looking difficult for those selling Medical or In Vitro Diagnostic equipment into the European market but things may be a bit easier in the UK where the options are greater and the timelines more flexible.

If you would like an update on what’s happening in medical regulations or you are having trouble with your Research Use Only, or Health Institution exemptions, we are lucky to have renowned legal specialist on the MDR and IVDR, Alison Dennis, of legal firm Taylor Wessing presenting this webinar. Alison will explain what’s going on, where the pinch points are and will answer your questions about your own products and issues.

To reserve your place, please click here