Learn how to apply Human Factors & Usability Engineering to devices development for safer, intuitive products & easier regulatory approvals.
The application of Human Factors, or Usability Engineering processes, into the development of medical devices leads to safer and more intuitive products. It also facilitates the regulatory approvals process. This helps to accelerate the adoption and spread of innovative medical technologies. This course will provide a “how to” guide, covering planning and implementation of usability studies, as well as designing and conducting Formative Evaluations and Summative Testing.
COURSE OVERVIEW
This webinar will cover the following topics:
- What is Human Factors?
- Why do it?
- When to do it?
- How does this align with the Medical Device Regulations?
- What is IEC 62366-1?
- How is it different from a clinical trial?
- What is involved?
- What sample size is needed?
For more information and to register, click here
Medilink Midlands Members can also benefit from a 50% reduction in admission price. Please enquire here