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UK Releases Draft Post Market Surveillance Requirements for Medical Devices

Leave a Comment / complaint management, Great Britain, incident response plan, Medical Device, MedTech, post-market surveillance, Quality/Regulatory, RC - EU MDR and IVDR, RC - Medtech Regulatory Resource Center / By

UK Releases Draft Post Market Surveillance Requirements for Medical Devices     The UK has released a draft of its proposed Post Market Surveillance Requirements for Medical Devices. If the draft regulations, “The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2023,” are approved, they will pertain to devices sold in England, Wales, Scotland and …

UK Releases Draft Post Market Surveillance Requirements for Medical Devices Read More »

Developing an Effective and Sustainable Regulatory Strategy for Today’s Global Market

Leave a Comment / AI, complaint management, EU MDR, Focus Article, From The Editor's Desk, Medical Device, medical device regulation, MedTech, post-market surveillance, Quality/Regulatory, RC - Quality & Regulatory Market Access Solutions, systematic literature reviews / By

Developing an Effective and Sustainable Regulatory Strategy for Today’s Global Market     Global regulatory demands for medical devices are increasing substantially, and regulatory teams are faced with the pressure of increased workloads and the need for more resources. To help regulatory professionals identify strategies and best practices in developing an effective and sustainable regulatory strategy …

Developing an Effective and Sustainable Regulatory Strategy for Today’s Global Market Read More »

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