EPTRI First Webinar Series: A JOURNEY IN PAEDIATRIC MEDICAL DEVICES

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The regulatory panorama of medical devices is changing according to the need of new laws disciplining this growing innovative field and the new European Regulation on medical devices which is mandatorily applied by the manufacturers from the 26th of May 2021.

The series A Journey in Paediatric Medical Devices: From Regulations to Clinical Case Studies and Patients Involvement’ is composed of three non-propaedeutic webinars that will deal with different aspects of the medical devices field: regulatory, clinical and developmental case studies, and patients involvement.

The first webinarThe evolution of the regulatory framework of MDs in Europe’ has been held on October 28th. It deepened in the general aspects on medical devices, absorption issues, the new requirements and changes compared to the older one and which are the specific needs to be covered according to the MDs Regulation to develop safer and adequate MDs for paediatric patients.

The second webinarA magnifying glass in the world of the medical device development’ will be held on 25th of November 2021 at 11.00 CET. It is tailored to the development of medical devices and will cover different MDs fields through the presentation of case studies.

The third and final webinarHealth technology designed for children with children’ will be held on 16th of December 2021 at 15.00 CET. Versatility is key to the development of health technology for children and young people so that it is adaptive to their social, physical and developmental needs. Co-design and development of medical devices with children and young people is key to adoption, acceptance and trust. This webinar will focus on the patient involvement in MDs development.

For more information and registration visit the dedicated web pages.