Tighter controls on medical device regulation

21/02/2012


The EU commission has issued a press release indicating that Commissioner Dalli has written to Member States asking for their co-operation within the existing legal framework to tighten controls to provide a better guarantee of the safety of medical technology, especially with high risk devices.

The proposed actions include:

-Verify the designations of Notified Bodies to ensure that they are designated only for the assessment of medical devices and technologies that correspond to their proven expertise and competence.

-Ensure that all Notified Bodies in the context of the conformity assessment make full use of their powers given to them under the current legislation which including the powers to conduct unannounced inspections.

-Reinforce market surveillance by national authorities, in particular spot checks in respect of certain types of devices.

- Improve the functioning of the vigilance system for medical devices, for example by giving systematic access for notified bodies to reports of adverse events; encouraging healthcare professionals and empowering patients to report adverse events; enhanced coordination in analysing reported incidents in order to pool expertise and speed up necessary corrective actions.

-Support the development of tools ensuring the traceability of medical devices as well as their long-term monitoring in terms of safety and performance, such as Unique Device Identification systems and implant registers.

This is the latest statement following the PIP breast implant problems.

Update provided by BSI, a Notified Body.


Commissioner Dalli's statements can be viewed on the EU Commissionís website


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