New Regulations on medical devices and in vitro diagnostic medical devices

QUESTIONNAIRE

The Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs (DG GROW) is launching a communication campaign on the new Regulations on medical devices (MDR) and in vitro diagnostic medical devices (IVDR).
The preparatory work of the communication campaign is ongoing. In this framework, we would like to ask your support, as a main stakeholder in this field, to help spreading the campaign messages and communication materials.

We kindly ask you to fill the form by the 18th of May 2018.

*are mandatory fields

1 - Are you and your members aware of the main changes brought by the Regulation on Medical Devices?
2 - Are you and your members aware of the main changes brought by the Regulation on In Vitro Diagnostic Medical Devices?
3 - Are you and your members aware of the transitional period (date of application and the different derogations) foreseen in the new EU Regulations on Medical Devices and In Vitro Diagnostic Medical Devices?
4 - Are you and your members aware of the main transitional provisions foreseen by the new EU Regulations on Medical Devices and In Vitro Diagnostic Medical Devices?
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