What does the acronym "CAP" stand for in a medical device context?

In the context of medical devices, the acronym "CAP" most commonly stands for "Corrective Action Plan." This is a systematic approach that organizations use to address and rectify non-conformities or issues related to products, processes, or systems within medical device manufacturing and maintenance. A Corrective Action Plan outlines specific actions to improve quality and ensure compliance with regulatory standards, thereby enhancing patient safety and device reliability.

The implementation of a CAP helps organizations identify the root causes of problems and develop actionable strategies to prevent recurrence. This is essential in the medical field, where equipment must meet rigorous safety and efficacy standards to protect patients.

Other terms associated with the acronym "CAP" may have specific uses, but "Corrective Action Plan" is particularly relevant when discussing processes for addressing issues in medical devices.