Medical-Device Usability – IEC 62366-1 as part of the development process

Medical-Device Usability –  IEC 62366-1 as part of the development process

The importance of usability in electrical and medical devices has grown dramatically. Good usability improves efficiency safety for medical device functionality and satisfaction with device use. Usability is also linked to demonstrating medical device compliance. Some of these requirements involve extensive documentation and a range of practical testing and specifications. This training will cover the usability process, specifically to the requirements of IEC 62366-1, but will also open up the design process from the perspectives of ISO 13485, IEC 60601-1-6 and ISO 14971 in the MDR/IVDR environment.  

Date and location:

April 28th, 2026
9 am – 4 pm (Registration and breakfast starting 8.40 am)

Juju Kampus, Takomotie 8, 00380 Helsinki

Training is conducted in Finnish.