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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WEBINAR: Medtech Regulatory Special Interest Group (SIG) – Product traceability and Unique Device Identification for the EU and Global Use

The next MedTech Regulatory Special Interest Group (SIG), delivered by regulatory affairs expert Richard Young and GS1 standards professional Chris Florey, will explore the requirements for product traceability and Unique Identification for the EU and Global Use, immediate and future considerations for a business. This webinar will cover: Richard Young, AcclaimBiomedical Consulting Ltd: Regulatory background Eudamed MDCG guidance so…

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How to get your Medical Device NHS Ready

Getting your Medical Device NHS ready is one of the biggest challenges companies face. With several obstacles to overcome and for some, unknown territory to cross, working with CHEATA (Centre for Healthcare Equipment & Technology Adoption) at Nottingham University Hospitals NHS Trust we have this great free to attend event.

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