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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Finland’s Eurofins Expert Services Oy is the latest Notified Body authorized to perform activities under...
The government bodies identified flawed reasoning behind the January notice with the proposed exemptions, which...
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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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