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

QA/RA

Medical technology has become so advanced, that Quality Assurance teams need tools that reduce the time they spend on training and role-based qualification management.   

As medical device regulatory agencies work on harmonization, so should the QA and RA teams that manage a global workforce, and supplier networks.

UL EduNeering develops solutions that reduce the time that QA and RA professionals spend on GMP training, while also producing measurable results that drive up quality.

  • ComplianceWire

    Hundreds of QA and RA professionals trust UL to manage global submission training, meet compliance objectives and build a stronger learning and development program. 

    Our Advisory Services team can work on your unique competency and process improvement projects, and our award-winning ComplianceWire platform is used by 400+ companies to manage both training and qualifications across the enterprise. This web-based platform meets both 21 CFR Part 11 and EU Annex 11 requirements.

  • Online Libraries

    Meet your GMP regulatory training requirements with the curricula provided in our GMP/QSR Medical Device Library. The library, authored by leading consultants such as EduQuest, contains 90+ self-paced courses that can be taken from virtually any learning system, and focus on topics such as 21 CFR Part 820 and 806, Part 11, EU MDD requirements, and more. Each course contains engaging interactive tools and built-in tests to measure retention and ensure knowledge transfer.

SOLUTIONS

  • Our experts will visit your site to deliver hands-on and in-depth workshops on GMP compliance, training matrix development, IT validation and dozens of other QA and regulatory issues.

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  • Learn why more than 350 companies worldwide rely on ComplianceWire, our award-winning LMS, to cost-effectively achieve their quality, compliance and performance development goals.  

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  • Leverage our combined web-based platform and Learning Services team to create a customized and cost-effective solution that delivers and tracks content to a targeted global community of non-employees such as physicians, clinicians, suppliers, distributors, regulators and more.

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  • Our clients save training course development time by using our 500+ standard online courses, which are written by industry experts, and can be customized to meet your needs.

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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.