In over 20 years of company history, novineon CRO has gained experience with all risk classes of medical devices and a wide variety of Notified Bodies. More than 250 projects per year on medical devices and in vitro diagnostics from the major medical specialties allow us to gain the big picture in Clinical Affairs. We are happy to pass this experience on to you: as free white papers, presentations on specific regulatory topics or individual workshops for your team.
Together with cooperation partners, novineon CRO regularly offers seminars on the most important topics related to the MDR and the IVDR. Upon request, we also conduct workshops with your team on specific issues.