This one-day intensive course enables greater understanding of the key requirements for technical documentation for medical devices, in line with the European Medical Device Regulation (MDR) requirements in Europe. The aim of the course is to enable manufacturers to:

  • Create robust technical documentation to demonstrate compliance to the MDR
  • Better understand regulatory requirements and Notified Body expectation, to prevent unnecessary delays to the certification process

Online training courses: Connected Learning Live
You can attend this training course classroom based and online. Do you prefer the convenience of an online training course? View here for the available dates or read more about Connected Learning Live.