Almost all the pharmaceutical company undergoes a quality system inspection method which involves an examination of the company’s CAPA system. This requires for FDA-regulated pharmaceutical firms which are stated in 21 CFR part 11. Qualityze Corrective Action system helps in automating routes, notification, delivery, escalation and also helps in approval of CAPAs and all related documentation. This software automates management of complete CAPA process from the state of initiation to investigation and all the way through closure. With this CAPA management software, you can get complete visibility into your corrective and preventive actions and their impact.