MHRA Launches a Consultation on Indefinite Recognition of CE-marked Medical Devices
The Medicines and Healthcare products Regulatory Agency (MHRA) has launched a public consultation on proposals to introduce indefinite recognition of CE-marked medical devices in Great Britain (GB). The initiative is intended to safeguard patient access and ensure the continued supply of safe and effective medical technologies. Approximately 90% of medical devices currently used in GB ...
Commission launches a public consultation and a call for evidence for EU Medical Devices evaluation
The European Commission has initiated a public consultation and call for evidence as part of a targeted evaluation of the EU legislation on medical devices and in vitro diagnostic medical devices. This consultation offers stakeholders the chance to share their views on the effectiveness of the current regulations and identify any potential shortcomings. The regulations ...
Consultation, EU, IVDR, MDR
