Acquire the Knowledge Needed to Enter New Markets
and Build a Stronger Quality Culture

MEDICAL DEVICE

Medical technology companies are seeking innovative methods to share compliance knowledge, educate new engineers on the latest standards, train global distributors, manage robust qualification models and develop their leaders of tomorrow. They also need to manage supplier audits and collaborate with all of the members of their value chain. That's why many of the world's leading Medical Device manufacturers rely on UL.

Our solutions enable you to meet regulatory, compliance and management development requirements that span the entire organization.


  • QA/RA

    Our GMP/QSR library focuses on more than 200 QSR regulations — focusing on 21 CFR Part 820, as well as global market access, IT validation, adverse events and other topics. Our US FDA-authored inspection and enforcement library can help your teams understand the FDA enforcement process.

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  • Corporate Compliance

    Corporate compliance teams turn to our libraries to educate all employees and contractors on key global ethics topics, such as anti-bribery and conflicts of interest, and industry topics such as AdvaMed Code. More Courses are available in multiple languages, so you can deliver training globally and produce audit-ready records in seconds.

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  • HR Leadership

    Deliver courses on key topics, such as harassment and discrimination policies, while also building professional development programs through our partner programs, which include the award-winning content from CrossKnowledge. 

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  • EH&S

    EH&S teams use our courses to satisfy OSHA, EPA and DOT requirements. Our Bloodborne Pathogens course is taken by more than 5,000 Health Care workers annually. Courses can be delivered to specific roles within the organization.

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  • UL EduNeering's Partnership with FDA Extended Until 2019

    The FDA's Cooperative Research and Development Agreement (CRADA) with UL EduNeering has created a collaborative partnership between the two organizations, resulting in courses developed with, and used by FDA inspectors and industry professionals worldwide.

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  • UL EduNeering maintains an Exclusive Compliance Partnership with AdvaMed

    UL serves as AdvaMed's exclusive online compliance partner, providing its members with educational resources to maintain regulatory compliance and professional knowledge. Those programs accommodate the needs of both emerging companies and well-established device firms.

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  • Brandon Hall Excellence in Technology Awards

    For SIX years running, UL has won an Excellence in Technology Award from Brandon Hall.  These awards were presented by Brandon Hall Research, one of the leading research firms in training and development.

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  • UL mdt

    UL mdt medical device testing GmbH is an EN ISO/IEC 17025 accredited-and GLP-certified testing institute that conducts performance and safety tests on medical devices for international device manufacturers. Specializing in clinical and non-clinical investigations and helping medical device manufacturers to obtain CE-marking and international market authorizations for their devices. UL mdt complies with applicable laws, guidelines, directives and standards for all of their services.

  • UL's Medical Regulatory Advisory Services

    With UL's Medical Regulatory Advisory Services Team, you have a regulatory partner who can help you understand the specific requirements needed for market entry and also determine the most efficient path to save valuable time and resources along the way.

  • UL Medical and Laboratory Services

    UL helps our customers prevent and resolve complicated quality issues that could lead to recalls, embargoes, bans and liability. We offer nonclinical testing; usability, EMC and performance testing; safety certification; and compliance training to help speed unrestricted access to the global market.