Reclassification of Medical Devices, upcoming revisions of EU regulations

Last May, the European (EU) Council published its position on the draft regulations for Medical Devices and IVD. Despite not being the final version, the EU Council’s position provides some insight and a better understanding of the regulation that the “Constitutional Triangle”—composed of the EU Commission, Parliament and Council—will discuss. Experts expect the final adoption of the new regulation to significantly revamp the current EU Directives regulating Medical devices (MD) and In vitro Diagnostics (IVD).

In this webinar, we will analyze the positions of the three main actors (EU Commission / Parliament / Council), focusing on the potential changes affecting the classification of MD and IVD devices.

The topics covered in this webinar include:

The state of the EU regulations and the processes they entail
The evolution of the EU regulations
Possible classification changes and the corresponding pathway for CE Marking
Potential impacts for MD and IVD manufacturers