Dia Pro prepares for the New Era

Dia Pro prepares for the New Era- We have Completed Our IVD-R Training

The European Union Medical Device Commission removes existing directives on in vitro diagnostic medical devices (98/79 / EC) and medical devices (93/42 / EEC). On 2017 May 5,  EU 2017/746 IVDR and 2017/745 MDR Medical Device Regulations were published in the EU official newspaper.

In this process, we have determined a road map for our organization. We have successfully completed the 'In vitro Diagnostic Medical Devices Regulation IVD-R 2017/746 and Medical Device Regulation MD-R 2017/745' trainings by Mr Maurizio Suppo from Qarad European Regulatory Services Company to complete the requirements of the regulations.