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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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Normal requirements for regulatory submissions or notification periods will be waived in certain cases impacted...
European Notified Body designation renewals eased ahead of new MDR date of application
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
We operate offices all over the world to deliver local expertise and a collaborative experience.
