What is contained in a Device Master Record (DMR)?

The Device Master Record (DMR) is a comprehensive set of documents that contains the specifications and procedures necessary for the production of a finished medical device. It serves as a central file that outlines everything essential to the manufacturing process, including design specifications, production processes, quality assurance measures, and packaging requirements. This detailed information is crucial for ensuring consistent manufacturing practices and compliance with regulatory standards.

The DMR encompasses various elements, such as drawings, material specifications, production process specifications, quality assurance procedures, and labeling. By having all these components documented, manufacturers can maintain product quality and ensure that their devices meet regulatory requirements for safety and effectiveness.

While other types of records may concern manufacturing history, adverse event reports, or lists of active pharmaceutical ingredients (APIs), these do not solely define the DMR, which is specifically focused on establishing the controls and parameters around device manufacturing.