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Medical Device Regulations Summit 2020 is focusing on EU MDR and IVDR overview, appropriate challenges and strategies for their overcome; company, ..
team and portfolio preparation to new regulations; technical documentation, labelling and clinical data adoption; risk management and quality management systems updates; compliance strategies; Unique Device Identification (UDI) system implementation; medical devices traceability and devices classification. Our meeting facilitates hands-on experience sharing with focus on early process development and scale up, occupational health regulations and safety standards and many others.
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