IQVIA CAPA Process

5 Steps to a Reliable CAPA Process

Is your CAPA process ready for its next FDA audit?

Learn how to maintain compliance and achieve operational excellence in your corrective and preventive action process:

Avoid 483s and Warning Letters by learning to identify common mistakes in CAPA management.
Understand how Risk Management feeds the Corrective Action process.
Involve the right people at the right point in the CAPA management process.

Discover More:

Fact Sheet: 5 Steps to a reliable CAPA process

Interested in exploring if your CAPA process is ready for its next FDA audit? Let’s Talk

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