The healthcare industry is changing and we have the breadth of expertise to help you evolve with it.
Comprehensive service offerings at every point in the product life cycle.
A platform of digital products to improve, simplify and automate RA/QA activities
Emergo by UL's new human factors tool - provides training, tools, and resources.
Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools.
The latest industry news and insights from our global team.
Stay informed with the most read RA/QA medical device newsletter.
TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.
Information and tools to advance your business.
Learn from our experts through live events.
Our global consulting team works from 20+ offices on six continents.
Resources and tools tailored to medical device professionals.
Our Emergo by UL expert outlines U.K. MHRA and Switzerland medical device regulatory updates in this on-demand webinar.
Discover how our HFR&D experts worked closely with Alexza Pharmaceuticals to improve the usability and use-safety of their device (Adasuve®) and its associated packaging and labeling.
In this complimentary webinar, our human factors engineering (HFE) experts outline the latest regulatory update from the U.S. FDA, published on Dec. 9, 2022.
This course will take someone who is already familiar with writing an HFE report to the next level.
This course will take someone who is already familiar with residual risk analysis to the next level.
This course will take someone who is already familiar with root cause analysis to the next level.
This course takes someone who is already familiar with usability test methods and might have conducted many test sessions, to the next level.
This course takes someone who is already familiar with use-related risk analysis to the next level.
This course takes someone who is already familiar with formative evaluation methods to the next level by addressing the nuances of conducting a formative evaluation.
Learn about designing effective instructions for medical products, including instructions that might take the form of instructions for use, quick reference guides, package inserts, online help and operator manuals.
Learn about a software user interface (UI) design process that is tailored to the development of medical products of various type.
Learn how to apply human factors engineering to medical products and the HFE process as it is prescribed by regulators and outlined in industry standards.
Learn how to convert the findings from user research into interface requirements.
Learn about HFE reports – what they are, when they are needed, and what they should include.
Gain insight into how people perceive risk, residual risk analysis and its use in medical device development. Sign up for courses on our HFE software platform, OPUS™.
Learn how Root Cause Analysis (RCA) is conducted to discover why problems occurred, and potentially mitigate such occurrences in medical products under development.
Understand usability testing and its key objectives, the differences between various usability tests, and the steps required to conduct usability testing. Sign up for courses on our HFE software platform, OPUS™.
Learn how to conduct a known problems analysis (KPA) to gain knowledge that helps eliminate use error vulnerabilities during the development of medical products.
Gain insight into risk analysis, particularly use-related risk analysis for medical device manufacturers, in this course.
Learn how to conduct user research, in order to develop safer, easier-to-use medical products, in this course.