The EU Commission published a survey in August 2023, this survey is due to close by the end of November 2023. It is only intended for stakeholders who are directly impacted by the regulatory changes for medical devices. That would seem to be a great number of organisations.
The object of this survey is to better understand the information needs around the EU Regulations on medical devices (MDR) and in vitro diagnostic medical devices (IVDR). Some would say the EU has done a poor job thus far in understanding the information needs in this regard.
Therefore, if you are a stakeholder who is directly impacted by the regulatory changes for medical devices, and has not yet taken this survey, we would encourage you to do so, just follow the link below, it should only take 5 minutes.
