Latest Notified Body Approval Helps Brexit-Proof EU Medical Devices Regulation
Executive SummaryAs the implementation deadline for the EU Medical Devices Regulation looms, the seventh notified body to be designated – BSI Netherlands – may hold the key to Brexit-proofing the new system.
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BSI Netherlands is the seventh notified body to be designated under the EU’s Medical Device Regulation. But this latest announcement is one of the most important yet.
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The Association of the European Self-Medication Industry (AESGP) warns that many self-care medical devices could fall through the cracks of implementing new EU regulations, as the deadline draws near.