On Tuesday, 20 August 2019 the European Commission closed its feedback period on safety and performance requirements for single-use device reprocessing. As the 26 May 2020 deadline for compliance with the new European Medical Device Regulation looms, we have arrived at a critical moment as European Member States now have sufficient information to safely reduce costs and “red bag” waste by adopting standards that will expedite single use device remanufacturing…
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