CAPA reports are critical in every regulatory inspection for medical devices, pharmaceuticals, and other life science companies worldwide including the EU and the US. They must be accurately written and should provide the auditors the information about the CAPA sub-system in the company. A poorly ...
This article educates about the CAPA form and also provides a free downloadable template for a CAPA form. What Are Corrective Action and Preventive Action (CAPA)? CAPA is a set of actions that your organization (medical devices, biotechnology, pharmaceuticals, food, beverages, etc.) maintains t...