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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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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
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Hosted by

Don Goetz-round
Presenter: Don Goetz

UX Design Manager, ICS / Boston UX
Milton-Yarberry
Presenter: Milton Yarberry

Director of Medical Programs, ICS
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Moderator: Jon Speer

Founder & VP of QA/RA, Greenlight Guru

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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.

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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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