Dassault Systemes, a world leader in 3D and Product Lifecycle Management (PLM) solutions, today announced the latest updates to the MatrixOne Medical Device Accelerator (MDA). The MatrixOne MDA manages Quality System Regulation (QSR)/ISO-regulated design processes, projects, documents and data, and is the only medical device-tailored solution built on an enterprise-class PLM platform that has been proven effective at the industry's top three device manufacturers.
Simplifying Global Compliance
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Biological Risk Evaluation and Management for Medical Devices
Report shows how the FDA incorporates the two ISO standards in its medical device development policy, how the EU version of the two standards differs in significant ways and how the EU Medical Device Regulation may require further changes in the European standards.
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