The HPRA will hold a Custom-Made Device (CMD) webinar in October 2023. The webinar is scheduled as a virtual event and will be hosted on the Microsoft Teams platform.
The webinar will give an overview of the Medical Devices Regulation (MDR) and how it applies to custom-made devices. It will focus on providing practical information regarding the application of the MDR for custom made device manufacturers.
The webinar will provide insights into key areas such as:
Classification
Conformity assessment
Vigilance reporting
Technical documentation requirements
