Latest Breaking News On - மருத்துவ சாதனம் ஒருங்கிணைப்பு குழு - Page 1 : comparemela.com

Photo by Darla Williams/ Getty Images The EU’s new regulation on medical devices finally came into full application today, following a year’s delay due to the COVID-19 pandemic. According to the European Commission, the Medical Devices Regulation (MDR) seeks to ensure a high level of public health and patient safety taking into account scientific progress. The regulation entered into force in May 2017, replacing the Medical Devices Directive. This transition period helped to avoid market disruptions and some transitional provisions are in place until 2025. In a statement on its website, the European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry (COCIR) welcomed the regulation, but raised concerns about the “plethora” of EU legislation that relates to medical devices.

Device coordination groupIrish medtech associationEuropean coordination committee of the radiologicalEuropean commissionMedical devices regulationMedical devicesEuropean coordination committeeRadio equipment directiveArtificial intelligence actNotified bodiesMedical device coordination groupMedtech associationசாதனம் ஒருங்கிணைப்பு குழுஐரிஷ் மெதிதேச் சங்கம்ஐரோப்பிய ஒருங்கிணைப்பு குழு ஆஃப் தி கதிரியக்கவியல்ஐரோப்பிய தரகு