Date07.04.2020 | 10:00 - 10:45


Available dates:

Clinical Data for Medical Devices

Join us for a complimentary webinar in which we will discuss the Regulation (EU) 2017/745 with a special focus on the collection, generation and evaluation of clinical data for medical devices.
Our expert, Dr. Kivia Pontes de Oliveira, will give you an insight on the following topics:

  • Requirements of the Regulation (EU) 2017/745 on clinical data
  • Identification of clinical data sources
  • Equivalence route and clinical investigation route
  • Post-Market Clinical Follow-up (PMCF) activities


Ticket Type Spaces
Standard-Ticket (kostenlos)