How to Use UX to Streamline Medical Device Product Cycles

FREE ON-DEMAND WEBINAR

How to Use UX to Streamline Medical Device Product Cycles

Human factors and good UX design have gained traction among medical device manufacturers and the FDA as imperative for reducing critical use errors and product recalls.

Unfortunately, many widely practiced UX design and software development processes don’t fit neatly into this stringent regulatory environment.

We've teamed up with Integrated Computer Systems, Inc. (ICS) to share their expertise in user experience design and provide actionable tips and best practices to help medical device companies with their product development efforts.

This free in-depth webinar will outline a process that not only fits within the regulatory parameters, but also is so effective that it shortens the typical product development cycle leading up to your regulatory submission.

Watch the webinar

How to Use UX to Streamline Medical Device Product Cycles webinar_Don-Goetz-Milton-Yarberry-ICS

Specifically, this webinar will cover:

FDA and the growing importance of human machine interfaces (HMIs) in regulatory submissions
Complexities at the intersection of UX design, software design and regulatory compliance
Development processes and the effect on quality and time-to-market
UX processes that truly work
The right tools to reduce critical use errors
Q&A Session

Who Should Attend?

UX Design Professionals and Managers
Software Development Professionals and Managers
Medical Device Executives
Regulatory Affairs Professionals and Management
R&D Engineers and Management

Hosted by

Presenter: Don Goetz

UX Design Manager, ICS / Boston UX

Presenter: Milton Yarberry

Director of Medical Programs, ICS

Moderator: Jon Speer

Founder & VP of QA/RA, Greenlight Guru

ICSlogo

About ICS / Boston UX

Whether you need help building a new device, revamping a legacy product or quickly solving a tricky development problem, ICS and Boston UX have you covered. We apply Design Thinking best practices to create compelling UX and highly usable UIs for Class I, II and III medical devices and applications. We also offer custom software development, IEC 62304 and 62366-compliant medical platform and services, and rapid development of embedded touch devices via GreenHouse by ICS. GreenHouse combines a UX-focused development process with a powerful software architecture in a test-driven environment to help you build superior products. Visit our website to learn more.

About Greenlight Guru

Greenlight Guru is the only Medical Device Success Platform (MDSP) for companies to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based software, Greenlight Guru is easier to implement, easier to use and designed to fit all medical device needs to enable innovative, safe and effective, True Quality medical devices. Visit our homepage to learn more.

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