| Date & Time | 10 November 2023 |
|---|---|
| Location | Online & Coimbra, Portugal |
This hybrid workshop is co-organised by the Medical Devices Regulatory unit from Instituto Pedro Nunes and TUV SUD Italy, responsible for TÜV SÜD’s operations in Portugal in the field of medical devices and in vitro diagnostics medical devices.
TUV SUD Italy is one of the Notified Bodies responsible for assessing the conformity of medical devices (MDs) and in vitro diagnostic medical devices (IVDs), as well as for granting the CE mark before they are placed on the European Union market. Together with the Medical Device Regulatory Unit, which specializes in regulatory issues for MDs and IVDs (including software as a medical device), the speakers will address the challenges faced by companies in obtaining the CE mark and how the process can be simplified.
The event will take place on 10 November 2023 at 2.30 p.m CET at the premises of the Pedro Nunes Institute (Coimbra, Portugal), as well as online. Click here to register.
