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The healthcare industry is changing and we have the breadth of expertise to help you evolve with it.

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Services

Comprehensive service offerings at every point in the product life cycle.

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RAMS

A platform of digital products to improve, simplify and automate RA/QA activities

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OPUS

Emergo by UL's new human factors tool - provides training, tools, and resources.

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Software

Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools.

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RADAR : Market Access Newsletter

Stay informed with the most read RA/QA medical device newsletter.

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TalkingPoints : Human Factors Newsletter

TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.

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Our global consulting team works from 20+ offices on six continents.

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HealthTech

Tech companies are bringing consumer-oriented connected health solutions to the regulated device market. We help tech firms design, implement, and run quality and risk management, clinical research, usability studies, and more.

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Latest HealthTech news

The latest industry insights from our global team.

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HFE knowledge task testing
  • Insights
Aug 22, 2023

Knowledge Tasks, Product Labeling Design and FDA Guidelines: Webinar Debrief

An overview of Emergo by UL’s approach to knowledge tasks to align with FDA expectations.

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  • Insights
Jul 14, 2023

What is the EU General Product Safety Regulation?

A look at the European General Product Safety Regulation and its impact on medical device economic operators
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  • Insights
Jul 13, 2023

The Bigger Picture: Serving life science companies

A look at our market access and human factors services in the context of comprehensive UL Solutions support for life science and healthcare companies
HFRD usability testing
  • Insights
Jun 22, 2023

What Does the Future Hold for Medical Device Usability Testing?

Medical device usability testing and the emergence of artificial intelligence
HFRD self selection study 0623
  • Insights
Jun 22, 2023

Self-selection Study Tips Part 2: Conducting Self-selection Studies

Key considerations for conducting self-selection studies for medical devices
HFRD MW 0623
  • Insights
Jun 21, 2023

Wiklund’s Perspective: Human Factors Engineering in Consumer Product Design

A look at the benefits of human factors engineering in consumer product design
2023 HFES
  • Insights
May 16, 2023

Emergo HFR&D at the 2023 HFES International Symposium on Human Factors and Ergonomics in Health Care

Part 2 of our report on key human factors engineering themes at the 2023 HFES conference
Graphic depicting correct and incorrect ways of wearing a mask
  • Insights
Apr 18, 2023

Webinar Debrief: Designing Effective Quick Reference Guides

Quick Reference Guides (QRG) to help users and patients understand Instructions for Use
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Information and tools to advance your business.

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  • White Paper

Understanding Europe’s In Vitro Diagnostic Medical Devices Regulation

Learn more about EU In Vitro Diagnostic Medical Device Regulations.
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  • White Paper

Early Communication with the FDA

Learn more about tips and other information to help you feel comfortable when corresponding with the FDA.
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  • Guide

Clarifying the Complexity of Human Factor Engineering

Expectations among regulatory bodies are growing just as HFE methods become more and more complex. How will you meet the requirements involved with marketing a medical device?
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  • On-demand Webinar

2023 South Korea Regulatory Overview

In this webinar, our Emergo by UL subject matter expert outlines the latest updates on medical device regulatory requirements in South Korea.
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