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.
The medical device regulatory landscape is evolving. We help you bring safer products to markets worldwide and maintain compliance – even if your device is novel or high-risk.
Emergo, with offices in Israel and worldwide, acts as an independent regulatory representative for medical device and IVD manufacturers.
Emergo by UL offers authorized regulatory representation for medical device companies looking to sell in the Malaysian market.
Let Emergo by UL assist you in evaluating the South Korean medical device regulatory framework as it applies to your device(s).
Emergo by UL can help you implement a vigilance system for adverse event reporting, recalls and post-market monitoring as required by the HSA.
The latest industry insights from our global team.
Good user interface (UI) design ensures that users have a valuable and enjoyable experience when interacting with an application. For mobile apps related to healthcare, a UI that prioritizes the user is of utmost importance as these applications are developed with the goal of improving patients’ lives and the level of care they receive.
Human factors specialists might opt to conduct an “out of the box” usability test of a medical device, such as for a home-use blood pressure monitor. In any case, it’s a great way to assess the user experience from the very start of product interactions.
Overcome challenges associated with conducting human factors usability tests with multiple analysts by practicing effective notetaking and data collection.
As Emergo by UL reported in August, the Ministry of Health in Israel, Medical Device Division, AMAR, announced (August 14, 2023) proposed amendments to the medical device regulatory system.
Learn about the FDA’s expectations for knowledge tasks and how to plan for and conduct knowledge tasks during usability testing.
In this webinar, our Emergo by UL expert outlines the latest updates on regulatory requirements in Japan.
Este webinar explica o conceito de Avaliação de Desempenho apresentado pelo IVDR 2017/746 e aspectos fundamentais a considerar para seu produto.
Learn how to improve feedback and reduce the nervousness in participants during medical device user research studies.
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.