Present a detailed case study of a significant GMP failure, outlining the sequence of events, regulatory findings, and the resulting corrective measures to look at what happens in the real world. Explore the importance of documentation, quality control, and equipment. Discuss how all of these need to be working properly.

Analyze the root causes, such as inadequate training or documentation lapses, and discuss the lessons learned that led to improvements in quality systems. Emphasize how such failures inform industry practices and underscore the importance of a proactive quality culture in preventing similar issues. Underscore that all of it works to help improve quality and safety of the products available.