5 Steps to a Reliable CAPA Process

1 Pages

IQVIA outlines best practices for corrective and preventive action (CAPA). Steps include documenting processes, leveraging trends to identify risks, solidifying root cause analysis, ensuring management involvement, and taking action to prevent recurrence. A strong CAPA program supports compliance, reduces risk of FDA 483 citations, enhances efficiency, and drives continuous improvement. Root cause analysis and leadership engagement are emphasized as critical for long-term operational excellence.

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5 Steps to a Reliable CAPA Process

5 Steps to a Reliable CAPA Process

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