Regulatory compliance: iQ IMAGE appoints new PRRC

As a medical device manufacturer, we are required by the Medical Device Regulation (MDR) to appoint a Person Responsible for Regulatory Compliance (PRRC). Effective immediately, this role is assumed by Mr. Erik Virtel who will continue to ensure the conformity of our medical devices from manufacture to release and beyond, taking care of post-market surveillance and vigilance reporting activities.

The PRRC is your contact of choice if you have experienced any malfunctioning, deficiency or non-conformity of our devices. In such a case, please report any suspected incident as quickly as possible. The easiest way to do so is through our medical device reporting page on our website. You can find it under menu item Services in section Medical Device Reporting. Alternatively, you may access the reporting forms directly.