Every life sciences company needs an effective corrective and preventive action (CAPA) system in order to meet FDA compliance requirements. It’s easy to understand the need for a system, but it’s not as simple understanding exactly what the FDA requires from your CAPA system.
We hope you find this list of FAQs to be helpful.
1. Does the FDA require that I use software to support CAPA?
No. The FDA doesn’t mandate that you use software. They do require that your CAPA system, whether...(read more)![]()
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