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TÜV SÜD is one of the few notified bodies that still has capacity for conformity assessment procedures for medical devices with the Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR). With the switch to EU regulations, manufacturers will have to have their existing products reassessed by 2027. This temporarily caused bottlenecks in the market. However, TÜV SÜD has…
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