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.
Get the latest global medical device regulatory news, insights from our experts and more.
European NLF compliance considerations for medical device manufacturers with machine, radio and PPE characteristics
How Malaysian medical device regulators are adapting to European Medical Devices Regulation compliance delays
A look at the European General Product Safety Regulation and its impact on medical device economic operators
A look at our market access and human factors services in the context of comprehensive UL Solutions support for life science and healthcare companies
A look at the trend of how European legislation regarding medical devices and other products takes the form of regulations more so than directives
The European Medical Device Coordination Group (MDCG) calls for limiting applications of Article 97 MDR for legacy devices now that MDR transition periods have been extended.
The roles of the Blue Guide and New Legislative Framework in European medical device regulatory systems
A use-related risk analysis (URRA) is an important cornerstone activity in your human factors engineering (HFE) process that is expected by regulators.
Key human factors engineering and usability issues for makers of OTC hearing aid devices on the US market
Key considerations for conducting self-selection studies for medical devices
Medical device usability testing and the emergence of artificial intelligence
A look at key benefits of integrating HFE into medical device PMS processes
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.