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
The latest industry news and insights from our global team. View All
India CDSCO publishes risk-based classification lists for six broad medical device categories
Australian regulators ease Conformity Assessment Requirements (CAC) for certain high-risk devices
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.
Learn from our experts through live events. View All
Our global consulting team works from 20+ offices on six continents. View All
