Simplifying Laboratory Access

In pharmaceutical laboratories, deviations from standard procedures are common, but handling them effectively is critical for regulatory compliance and quality assurance. 🔹 How does your lab document and investigate deviations? 🔹 What root cause analysis techniques do you use? 🔹 Any specific formats or tools (like 5 Whys, Fishbone) that have helped streamline the process? Would love to hear your workflows, audit experiences, and how you train staff for deviation handling.