In the framework of the new Medical Device Regulations,

you will find below the Team-NB members’ intention to submit their application to be designated against MDR and/or IVDR. The Team-NB notified body members have a double advantage to pass their designation audit :   The peer review against the Code of Conduct which requirements are ahead of the today ones. The working groups reviewing [...]

2022-04-08T18:20:28+01:00

Medical devices : deal reached on new EU rules

The political agreement reached is still subject to the approvals (Council's Permanent Representatives Committee and Parliament's ENVI committee). The agreed two draft regulations are expected to achieve a twofold aim : making sure that medical devices and in vitro diagnostic medical devices are safe while allowing patients to benefit of innovative health care solutions in [...]

2022-04-08T18:20:29+01:00
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