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CAPA Management with Labwise

Labwise is a comprehensive quality management software solution that enables integrated CAPA Process Management. Labwise provides a comprehensive corrective and preventive  actions workflow as part of its enterprise quality management solution. The CAPA solution is integrated with all other core quality management processes. Corrective Action and Preventive Action (CAPA management) is one of the most daunting tasks of any quality-minded organization. FDA, ISO, EMEA, and other regulations and standards mandate a systematic approach to managing corrective and preventive actions.

While all organizations hope to avoid the root causes that necessitate corrective actions, reality dictates otherwise. Because defects, deviations, or any other gaps that trigger the need for a CAPA can come from a myriad of sources (documents, training, products, etc.), CAPA management has become the core process of a well-established compliance and quality program.

The CAPA module is an integral part of the Labwise Suite. It may be used as a stand-alone module in small organizations or integrated with other processes such as non-conformances, audits, training, complaints and others. The Labwise  CAPA module allows organizations to create a single configurable workflow to handle the entire lifecycle of the CAPA from the triggers that can auto-launch the corrective action to the final sign-off. If your company prefers, multiple workflows can be developed also – without vendor or IT support.

The Xybion Labwise suite delivers a comprehensive platform for GRC and quality management. Our comprehensive solution includes embedded best practices and flexibility for deployment in any systems environment. Labwise is seamlessly integrated with standard enterprise technologies including Microsoft, Oracle,  Documentum and others to ensure compatibility with most systems environments.

The key benefits of our overall solution are:  

  • Enterprise Platform as a Service
  • On-Premise, SaaS Deployment Options
  • Advanced Integrated Technologies
  • Flexible Process Control Engine
  • Compliant With Current Regulatory Guidelines

What is CAPA?  – CAPA is a concept within current good clinical, lab and manufacturing practices (cGxP), and numerous ISO business standards. It focuses on the systematic investigation of the root causes of identified problems or identified risks in an attempt to prevent their recurrence (for corrective action) or to prevent occurrence (for preventive action).

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