FDA Corrective Action Preventive Action (CAPA)
MasterControl's FDA Corrective Action Preventive Action (CAPA) software allow organizations to streamline corrective and preventive action according regulations stipulated by the FDA.
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Meeting the Requirements for FDA CAPA (Corrective Action Preventive Action)
FDA CAPA software from MasterControl automates the entire process for corrective action and preventive action. Every activity having to do with CAPA is linked to all other compliance-related processes. MasterControl CAPA automates activities such as routing, notification, approvals, and escalations. The complete system for FDA CAPA is electronically managed by MasterControl, starting with the opening of a CAPA and the CAPA investigation, and ending with the closure of the CAPA.
MasterControl offers a "continuous validation" approach along with the solution for FDA corrective action preventive action, which dramatically reduces the time, resources, and costs involved in validation of the software. Product training and technical support for FDA corrective actions are also available.
About MasterControl's FDA Corrective Action Preventive Action
MasterControl Inc. is a global provider of GxP process, quality audit, FDA CAPA, and document management software solutions for life science companies. MasterControl products are easy to use, easy to deploy, easy to validate, and easy to maintain. They incorporate industry best practices for automating and connecting every stage of the product development cycle, while facilitating regulatory compliance. By combining an integrated platform with a continuum of risk-based FDA corrective action preventive action software validation products and services, system can be managed effectively and efficiently.
To Learn More on FDA CAPA
To learn more about FDA corrective action preventive action, corrective actions, and the corrective action report, please feel free to contact a MasterControl representative.
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