Our partner, Evnia, held a webinar on the European Requirements for the CE-Certification of Medical Devices and In Vitro Diagnostics according to on 10th February 2025.
The webinar was designed to support medical device developers, regulatory professionals, and industry stakeholders in navigating the Medical Devices Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR) under European law (EU MDR 2017/745 & EU IVDR 2017/746). Led by Evnia’s regulatory experts, Vicky Valla and Vassiliki Basinou, the session offered practical guidance on achieving CE certification, understanding regulatory converging and diverging concepts, and overcoming implementation challenges across Europe.
Participants gained valuable insights and had the opportunity to engage in a Q&A session, ensuring a deeper understanding of the CE certification process and regulatory landscape.
