Corrective and Preventive Action (CAPA) Procedure for GMP
GMPSOP
MARCH 17, 2023
Immediately communicate the incident to stakeholders and initiate an internal laboratory investigation. You may have to qualify a new supplier, re-train the employees on operating procedures, re-validate the method to make it robust, or improve storage conditions, etc. ISO 9000:2005 Sec. Ideally, you should halt further testing.
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