Examine best practices for managing deviations from established processes, emphasizing the importance of clear procedures and thorough documentation. Explore the crucial role of Standard Operating Procedures (SOPs) as the rule book for consistent operations and how deviations from these written instructions are identified and addressed. Discuss how deviations are documented, including details such as who spotted the deviation, what went wrong, when it happened, and where it occurred, ensuring a clear, accurate, and traceable record.

Uncover how thorough documentation, root cause analysis, and corrective action planning are employed to investigate and resolve non-conformances. Dive into the significance of timely deviation reporting, continuous monitoring, and proactive risk mitigation strategies in maintaining process integrity and ensuring that quality issues are addressed systematically to prevent recurrence. Discuss how robust corrective and preventive action (CAPA) systems help organizations not only fix immediate problems but also prevent them from happening again, focusing on trends and potential issues before they become full-blown deviations. Learn about the importance of GMP in labs and clinical trials to see how the best ways to handle deviation.