(IN BRIEF) SGS Belgium NV has been designated as a Notified Body under the EU’s In Vitro Diagnostic Medical Device Regulation (IVDR), expanding Europe’s limited capacity for regulatory assessments. Approved by the European Commission and Belgian authorities, the Antwerp-based facility … Read the full press release →
Posted in Belgium, Business, European Union, Financial, Government, Healthcare, Industrial, Investment, Management, News, Switzerland, Technology
Tagged AFMPS, CE compliance, CE marking, diagnostics, EU 2017/746, EU regulatory compliance, European Commission, FAGG, Geofrey De Visscher, in vitro diagnostic medical devices, ISO 13485, IVDR, IVDR certification services, MDR, MDSAP, medical device certification, NANDO database, Notified Body 1639, partnership, patient safety, regulatory affairs, SGS Antwerp, SGS Belgium, UKCA
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