Third Party Funds Group - Overall project
Acronym: MDR Seminar
Start date : 01.01.2020
End date : 31.12.2020
Website: https://www.zimt.fau.eu/wissenschaft/medical-devices-law-seminar/#collapse_1
The new European Medical Device Regulation (MDR) has already entered into force, and all medical technology entrepreneurs and innovators need to familiarize themselves with the new requirements for the European approval process. This certificate course will offer a combination of knowledge acquisition in a university setting and the character of a seminar with the opportunity to make contacts with participants as future specialists. Healthcare and industry professionals, entrepreneurs, MedTech researchers, and students will be targeted for participation and will be eligible to receive ECTS (or CME) credits for 10 different seminar days covering topics including MDR fundamentals, country-specific reimbursement, risk management, clinical evidence, software for medical devices, eHealth, usability, post-market surveillance, and General Data Protection Regulation.