Categories
Topic

What is Corrective and Preventive Action (CAPA)?

The FDA, the US federal agency, lists Corrective and Preventive Action (CAPA) as one of the most crucial quality systems. The purpose of implementing CAPA is to identify, analyze, and control hazards, defect and nonconformities in order to ensure quality finished products.  Before we go into the details, though, let’s cover the basics! What is […]