Medical device usability engineering – managing use related risk, training, Helsinki

The training, arranged in co-operation with USBIMED (Finland) and Curiolis, Inc., (USA), is prioritized especially for medical device (including software) and digital health product companies or research projects and healthcare units developing these products as manufacturers. It is also suitable for design professionals who work with usability of safety critical systems theme in practice or are leading these activities.

Time: 26 September 2019, 8:30-16:30
Place: Tapahtumatalo Bank, Helsinki
Instructor: Curiolis, Inc. (Jonathan Kendler)

Registration is open.

Aim of training day

To learn what is required from medical device usability by EU regulations and by US FDA. To find out the status and content of standards and guidance for compliance. To deepen the understanding of the relationship between risk management and usability. Training covers also overview of typical usability engineering techniques, concentrating more deeply into medical device (including software) usability testing as a crucial method of evaluation. This practical training day includes best practice examples of medical device usability engineering and user interface design.

Registration and cancellation policy

  • Fee: 390 € (alv 0%) per participant. VAT 24 % will be added to price. The fee includes: training, course materials, lunch and both coffee breaks. Participation fee will be billed after the event.
  • Registration by 29.8.2019 required.
  • Cancellation by 29.8.2019 at latest, free of charge
  • Cancellation during 30.8. – 13.9.2019 payment 50 %. Substituting colleague may be announced.
  • Cancellation 14.9.2019 or later – full payment. Substituting colleague may be announced.

Check the program and more information here.

This training day is arranged in co-operation with USBIMED (Finland) and Curiolis, Inc., (USA).

 

Contact person

Terhi Holappa
Entrepreneur (CEO), USBIMED
terhi.holappa@usbimed.fi
+358 40 5595 726

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