A growing number of medtech companies are embracing User Experience (UX) Design and Human Factors Engineering (HFE) — not just to meet FDA regulations, but also to create more intuitive, more usable, and holistically better products. These practices required to promote safety and efficacy also provide an opportunity for your company to quickly deliver products that are more innovative, which can be a key differentiator in the competitive medical device market.
This webinar will be delivered jointly with our partners, human factors experts at UserWise, and will answer the questions: what is Human Factors Engineering and why is it important? We’ll also cover:
Human Factors guidance and regulations
Human Factors Engineering process overview
Differences between regulatory usability and UX
How to use UX to feed regulatory development
If you’re looking to get ahead in the medical device market, download now!
One of the most effective software engineering approaches involves separating the user interface (frontend) from the business logic (backend), especially when it comes to developing embedded-devices. This practice makes it far easier to code for a single specific functionality versus coding an overall product.
In this webinar we’ll explain not only what’s involved in separating the UI from business logic in your next Qt project, but explore some of the key benefits of this approach, including:
Parallel development
Modularity
Enhanced testability
Accelerated development
Architecture that easily accommodates future changes
We’ll also touch on a few of the drawbacks, chief among them the need to implement new strategies for independent testing, build and deployment — tasks that take extra time and resources.
