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.
Our team of experts has compiled case studies, white papers, process charts, guides, eLearning courses, market data, videos and additional resources for your reference.
Understand usability testing and its key objectives, the differences between various usability tests, and the steps required to conduct usability testing in this course.
Learn how to conduct a known problems analysis (KPA) to gain knowledge that helps eliminate use error vulnerabilities during the development of medical devices.
Gain insight into risk analysis, particularly use-related risk analysis for medical device manufacturers.
Learn how to conduct user research in order to develop safer, easier-to-use medical products in this course.
Understand how HFE's user-centered design process supports the development of safer medical devices.
This certificate's series of eight courses provides HFE professionals with a solid working knowledge of human factors engineering for medical devices.
In this complimentary webinar, we review the resources you’ll require and the steps you should take to complete your path to market in Japan.
Join the HFE experts at Emergo by UL as they discuss both tips to follow and pitfalls to avoid when writing user interface requirements.
Join the HFE experts at Emergo by UL as they discuss regulator expectations for electronic instructions for use (eIFUs).
The new JIS T62366-1:2022 standard comes with updated requirements on usability engineering for medical devices.
Watch this webinar to learn the anticipated updates to the EU IVDR 2017/746 and EU MDR 2017/745, what to look out for from the UK Medicines and Healthcare Products Regulatory Agency (MHRA) and the next steps for Switzerland.
Review recently released and expected guidance documents from the US FDA, the growing use of real-world evidence and regulatory science tools in submissions, and expectations for 2022 and beyond.
Thanks for your interest in our products and services. Let's collect some information so we can connect you with the right person.
We'll review your message carefully and get back to you as quickly as possible. To help ensure that you receive our reply, please add our domain @emergo.ul.com to your list of approved contacts.