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Compliance & Regulatory Review

Regulatory affairs is an integral part of any company looking to successfully sell their medical products in today’s market. NeoMedix's technical knowledge of medical devices can assist your organization in working with the FDA and/or a Notify Body (ISO). Neomedix has extensive experience in preparing FDA submissions, and/or design dossiers. NeoMedix can help, every step of the way, to insure the successful market launch of your new product.


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