Iri-Ce
IRI-CE is a consulting agency specializing in Regulatory Affairs and Quality Management entirely dedicated to medical devices. With our expertise in Regulatory Affairs, we support your teams and your company in their projects to obtain CE marking and regulatory authorizations. Our complementary expertise in Quality Management allows us to support your teams and your company for their certification projects (ISO 13485, MDSAP, FDA). Our agency offers a personalized approach adapted to your products/services and to the size of your company.
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