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.
An in-depth look at industry topics.
General principles of GDPR and actions manufacturers can take to gain or maintain compliance.
Secure data management to meet HIPAA, PHI, and requirements of Covered Entities or Business Associates.
Secure data management to meet HIPAA, GDPR requirements and achieve regulatory compliance.
Use this short checklist to assess what your medical device company needs to do to comply with the EU MDR.
This guide helps explain how to prepare a Clinical Evaluation Report for medical devices as well as what required updates need to be made.
Gain deep insights into Human Factors Engineering (HFE) and its applications to medical device design by reading these publications.
This brief checklist will help you to determine how to bring your in vitro diagnostic medical device company into compliance with the EU IVDR.