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We have deep expertise with a range of product types, including combination and borderline products.
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A platform of digital products to improve, simplify and automate RA/QA activities
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The National Medical Products Administration (NMPA) and Center for Medical Device Evaluation (CMDE) have issued...
A look at the ISO 20916 standard for IVD device clinical performance studies
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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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