Do you know capa process , validation deviation process

Question

Accepted Answer

Yes, I am familiar with CAPA process and validation deviation process.

CAPA (Corrective and Preventive Action) process is a quality management system used to identify, investigate, and resolve quality issues.
Validation deviation process is used to document and investigate any deviations from the validated process or procedure.
Both processes are important in ensuring quality and compliance in various industries, including pharmaceuticals and medical devices.
Examples of CAPA process include identifying root cause of a quality issue, implementing corrective actions, and monitoring effectiveness of the actions taken.
Examples of validation deviation process include documenting any deviations from the validated process, investigating the cause of the deviation, and implementing corrective actions to prevent recurrence.

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