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DEPARTMENT OF HEALTH & HUMAN SERVICESPublic Health Serviced and Drug Administration 10903 New Hampshire Avenue Document Control Center WO66G609 Silver Spring, MD 209930002December 22, 2016Eli Lilly

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Director-Regulatory CMC Devices refers to the individual responsible for overseeing regulatory affairs related to manufacturing, control, and quality of medical devices.

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The Director-Regulatory CMC Devices is typically required to file this documentation as part of regulatory compliance.

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The purpose of Director-Regulatory CMC Devices documentation is to ensure that medical devices meet regulatory standards for manufacturing, control, and quality.

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Information regarding manufacturing processes, quality control measures, and regulatory compliance must be reported on Director-Regulatory CMC Devices forms.

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