The European Association of Medical Device Notified Bodies, also known as Team NB, has proposed the issuance of a conditional ...
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New report reveals ongoing industry challenges around EU’s IVDR and MDR complianceA new report by trade association MedTech Europe has revealed that the struggle for manufacturers to meet the requirements of the EU’s Medical Device (MDR) and In Vitro Diagnostics Regulation ...
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However, further research is required. The results are also a success for the MDR & IVDR Competence Center (MIK) of the NMI ...
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