Usability and ergonomics have become important quality and performance features of medical devices. The two standards EN 62366-1 and EN 60601-1-6 are harmonized under the Medical Device Directive (93/42/EEC and 98/79/EC) and describe how the usability requirements are to be considered in the development process of medical devices.
Use our expert knowledge already in the idea phase and feasibility analysis. This is where the ergonomics and usability process begin, not the finished product! The integration of the user and customer into the development process is the key to success.
NSF International is a member of the working group IEC 62A/ISO 210 JWG4 and is currently working on the standards IEC 62366-1 and IEC 62366-2. Use our network for your future development projects.