Matrix Medical Devices LLC is a leading regulatory and quality partner for the medical device industry, specializing in US FDA and International Regulatory approvals. With a senior-level team experienced in all aspects of the commercialization process, they offer reliable and efficient program management, FDA and ISO Quality System infrastructure, and support for submission and compliance requirements in domestic and international markets.
Matrix Medical Devices provides a robust regulatory and quality foundation, enabling an accelerated product commercialization process. Their services include FDA regulatory strategy, gap analysis, and procedures, as well as establishing a sound quality foundation and offering expertise in program management and clinical studies. With over 125 years of combined experience, Matrix Medical Devices is dedicated to providing success and stability for their clients.
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