In this compelling Deep Dive, we explore the unglamorous but absolutely essential world of medical device documentation. From design inception to post-market surveillance, documentation isn't just red tape—it's the backbone of compliance, traceability, and patient safety. This episode introduces listeners to the U.S. FDA's regulatory foundation in 21 CFR Part 820 and shines a spotlight on ALCOA+ principles: the industry gold standard for ensuring that every action, every test, and every result is accurate, trustworthy, and audit-ready. Through clear examples and engaging conversation, the episode maps how documentation supports every phase of a device's life, from design through manufacturing to corrective actions and recalls.

Listeners are guided through the three cornerstone documents of medical device quality—Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR)—with an emphasis on how each connects design intent to execution and oversight. The narrative expands to include digital documentation, introducing 21 CFR Part 11 requirements for electronic records and audit trails. With real-world stakes, like product holds due to missing signatures, the episode demonstrates how documentation failures can halt entire product lines. Most importantly, it reframes GDP as a cultural mindset—a proactive approach to quality rather than a bureaucratic burden. It’s a must-hear for anyone looking to understand the DNA of device quality systems.