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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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China’s National Medical Products Administration (NMPA) has started a public consultation on its evaluation of...
European regulators issue recommendations for integrating UDI into medical device, IVD QMS processes
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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
We operate offices all over the world to deliver local expertise and a collaborative experience.
