Webinar: EU Perspective on Medical Devices in 2021 Analysis of the new requirements by MDR & BREXIT In this webinar we will cover: MDR requirements & timeline Notified Bodies Technical Documentation UK Guidelines & timeline UKCA UK Responsible Person Register and get the recording! Sign Up! Webinar: Classification rules under IVDR and Covid-19 derogation lists & database View Post Fighting a threat to public security: Regulation on marketing and use of explosives precursors View Post