Take an in depth look at the application of mandated requirements for usability engineering, with our Human Factors Masterclass in partnership with Thay Medical.
Medilink WM and Thay Medical bring to you a practical Masterclas designed around the delegate. These intimate sessions are created to maximise learning outcomes and designed to promote interaction and group discussions.
The course will –
-Give an overview of the current human factors and usability engineering processes for medical device developments.
-Give an overview of the three most frequently used human factors and usability engineering processes guided by IEC 62366-1, the US FDA and the UK MHRA.
-Show how the new European Medical Device Regulation (MDR) requests further evidence of use safety and reduced use-related risk in specific areas of medical devices and systems.
-Encourage the use of a risk-based approach to scale and incorporate human factors and usability engineering into a medical device development.
-Show examples of good and less good usability in medical devices and similar products.
-Show how to predict the level of use-safety a medical device may have whilst it is in development.
-Show how to perform compliant and effective human factors and usability tests globally.
-How to compile the Human Factors or Usability Engineering File effectively.
Medilink Members: £199
Non Medilink Members: £250
*Early Bird discount available. Save £15 on all bookings made before 25 May 2018*
For more information please contact:
Vanessa Bailey, Events Coordinator at – email@example.com