A number of different topics are relevant for the implementation of the Medical Devices Regulations: the number of areas is vast and includes, among others:
- notified bodies
- Unique device identifier (UDI)
- reprocessing
- harmonised standards
- combined studies
- counterfeiting
- custom made devices
- the European medical devices nomenclature (EMDN)
- in house medical devices
- software
For further information on Topics of Interest
