01Regulatory alignment with ISO 13485, FDA 21 CFR 820.100, and EU MDR standards.
02End-to-end CAPA lifecycle management from initiation to effectiveness verification.
03Specialized investigation protocols for quality, safety, and process deviations.
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05Multiple RCA methodologies including 5 Whys, Fishbone, and Human Factors Analysis.
06Automated trend analysis and performance metrics like Cycle Time and Recurrence Rate.