Latest Breaking News On - Medical devices regulation - Page 1 : comparemela.com

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 kingdomInternational medical devices regulators forumNational strategyNational ai strategyMedical devices regulationSocial careMachine learningUnited 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 generalUnited statesBruxelles capitaleEtcheverry escuderoNita farahanyInternational centerOrganisation for economicUniversity of texas at austinDuke universityEconomic co operationAnticipatory governanceEmerging technologiesFuture generationsGeneral data protection regulationGeneral product safety regulationMedical 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 szymaNational cardiac societiesEuropean health data spaceRegulatory affairs committeeStakeholder forumEuropean society of cardiologyEuropean parliamentEuropean societyAffairs committeeMember statesMedical devices regulation

CE Marking for Medical Devices - What Does It Mean?

CE Marking for Medical Devices - What Does It Mean?
marketbusinessnews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from marketbusinessnews.com Daily Mail and Mail on Sunday newspapers.

United statesKenneth shawEuropean economic areaEuropean conformityTechnical fileDesign dossierNotified bodyMedical devices regulationVitro diagnostic regulationMedical deviceNotified 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 unionEuropean commissionDevice coordination groupEuropean databaseMedical devicesVitro diagnostic medical devices regulationDiagnostic medicalVitro diagnostic medical device regulationMedical devices regulationMember statesMedical device coordination groupMember stateMedical device regulation