Live Breaking News & Updates on Medical Devices Regulation

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UK MHRA Publishes AI Regulatory Strategy | Hogan Lovells

On 30 April 2024, the UK Medicines and Healthcare Products Regulatory Agency (MHRA) published its strategic approach to AI and the steps it is taking to implement the UK Government's AI. ....

United Kingdom , International Medical Devices Regulators Forum , National Strategy , National Ai Strategy , Medical Devices Regulation , Social Care , Machine Learning , United Kingdom Medical Devices Regulations ,

Science ministers commit to better forecast and steer disruptive new technologies

Science ministers from across the world have endorsed a new approach to how new technologies are regulated, warning that governments need to foresee and steer breakthroughs, rather than being caught on the back foot and reacting to problems after they emerge. ....

France General , United States , Bruxelles Capitale , Etcheverry Escudero , Nita Farahany , International Center , Organisation For Economic , University Of Texas At Austin , Duke University , Economic Co Operation , Anticipatory Governance , Emerging Technologies , Future Generations , General Data Protection Regulation , General Product Safety Regulation , Medical Devices Regulation ,

ESC Hails EHDS Provisional Deal, Urges Harmonised Implementation

ESC Hails EHDS Provisional Deal, Urges Harmonised Implementation
miragenews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from miragenews.com Daily Mail and Mail on Sunday newspapers.

Piotr Szyma , National Cardiac Societies , European Health Data Space , Regulatory Affairs Committee , Stakeholder Forum , European Society Of Cardiology , European Parliament , European Society , Affairs Committee , Member States , Medical Devices Regulation ,

CE Marking for Medical Devices - What Does It Mean?

CE Marking for Medical Devices - What Does It Mean?
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United States , Kenneth Shaw , European Economic Area , European Conformity , Technical File , Design Dossier , Notified Body , Medical Devices Regulation , Vitro Diagnostic Regulation , Medical Device , Notified Bodies ,

In vitro diagnostics and the European Database on Medical Devices (EUDAMED) - guide — EUbusiness.com

The European Commission proposed on 23 January more time for companies to apply the In Vitro Diagnostic Medical Devices Regulation (IVDR), under certain conditions, as well as measures to enhance transparency in the medical device sector including speeding up the launch of some elements of the European Database on Medical Devices - EUDAMED. ....

European Union , European Commission , Device Coordination Group , European Database , Medical Devices , Vitro Diagnostic Medical Devices Regulation , Diagnostic Medical , Vitro Diagnostic Medical Device Regulation , Medical Devices Regulation , Member States , Medical Device Coordination Group , Member State , Medical Device Regulation ,