The healthcare industry is changing and we have the breadth of expertise to help you evolve with it. View All
We have deep expertise with a range of product types, including combination and borderline products.
Comprehensive service offerings at every point in the product life cycle.
A platform of digital products to improve, simplify and automate RA/QA activities
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SFDA UDI compliance timeframes for medical devices extended to 2022, 2023
European MDCG guidance identifies MDR compliance requirements for legacy devices based on task force report
Resources and tools tailored to medical device professionals. View All
Europe's Medical Devices Regulation (MDR) goes into effect in May 2020, and we want you to be prepared. Meet our MDR team and get free educational resources on the MDR.
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Our global consulting team works from 20+ offices on six continents. View All
Emergo by UL consultants are ready to fully support your CE Marking transition from the In Vitro Diagnostic Medical Devices Directive (IVDD) to the IVDR.
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