WEBINAR: An update on current changes to MDR, IVDR & Role of the Person Responsible (PRRC)

The next MedTech Regulatory Special Interest Group (SIG), hosted by regulatory affairs expert Richard Young, from AcclaimBiomedical Consulting Ltd, will provide a comprehensive update on the current Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) landscape, plus an overview of the requirements and practical considerations needed within a company to meet regulatory compliance.

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