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New Guidance on the Application of Article 97 of the MDR to Legacy Devices Certified under the MDD or AIMDD

European Commission Announces Intention to Introduce Three-Year Extension to the MDR Transition Period

Change is Coming for Software and AI Medical Devices in the UK

Change is Coming for Software and AI Medical Devices in the UK
Notified body capacity needed! MDCG proposals recognize need to increase notified body capacity to ensure device availability

Notified body capacity needed! MDCG proposals recognize need to increase notified body capacity to ensure device availability
