May 1, 2023
Europe
The new article highlights the aspects related to cybersecurity for software-based medical devices intended to be marketed and used in the UK. Table of Contents The Medicines and Healthcare Products Regulatory Agency (MHRA), a UK regulating authority in the sphere of...
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Apr 10, 2023
Europe
The new article highlights the aspects related to post market activities intended to ensure continuous safety and proper performance of medical devices allowed to be marketed and used in the country. Table of Contents The Medicines and Healthcare Products Regulatory...
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Mar 23, 2023
Europe
The new article describes in detail the aspects related to the existing premarket requirements and the improvement they require. Table of Contents The Medicines and Healthcare products Regulatory Agency (MHRA), the UK regulating authority in the sphere of healthcare...
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Mar 2, 2023
Europe
The new article highlights the aspects related to the classification of medical devices the UK authority intends to improve by the virtue of amending the existing regulatory framework. Table of Contents The Medicines and Healthcare products Regulatory Agency (MHRA),...
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Aug 8, 2020
Europe
MedTech Europe, a European association of medical device manufacturers and other industry representatives, has published a call to action related to the virtual inspections of the manufacturing facilities. Virtual Audits: Regulatory Background First of all, it is...
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