Corrective Action Software Systems

Corrective Action software systems help regulated companies effectively manage the entire CAPA process according to FDA and ISO best practices.

Regulated companies are increasingly recognizing the benefits of employing corrective action software systems and integrating it with process and event management software for managing document control, change control, employee training, and other processes.

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Product Data Sheet: MasterControl CAPA™
Product Data Sheet: MasterControl QEM CAPA Workshop
Product Data Sheet: MasterControl QMS and QEM Systems
Interactive and Live Demonstration: MasterControl Quality Suite Demonstration
White Paper: Simplifying CAPA: Seven Steps
White Paper: Does Your CAPA Need a CAPA?
White Paper: How to Kick-Start Your CAPA Process
Q&A: The CAPA Engine and Your QMS System - Is it Driving Your Company Forward?
Webinar: The Importance of Effective CAPA and Root Cause Analysis Processes



Implementation and Validation Tips for Corrective Action Software Systems

FDA 21 CFR part 11 requires that life science companies ensure the accuracy, reliability, and consistent performance of their electronic system. ISO certified companies and manufacturers also need corrective action systems to meet best practice guidelines. The corrective action software from MasterControl ensures an accurate and reliable system for correction action or CAPA processes. It also ensures consistent performance. The solution for CAPA is easy to use, easy to deploy, easy to validate, and easy to maintain. Features of the corrective action software systems (MasterControl CAPA) include:

  • Best-practice electronic forms
  • Connected quality processes
  • Advanced analytics and reporting
  • Increase efficiency through automation
  • Centralized repository
  • Advanced tracking
  • Easy web-based access
  • Integration with other quality processes
  • Form-to-form launching
  • Continuous validation
  • Product training
  • Technical support

MasterControl Education Center for Corrective Action Systems

MasterControl's Education Center is a comprehensive site dedicated to providing life science companies with the educational and research materials they need to make the right decisions about corrective action software and other quality solutions.

Life science companies can also subscribe to MasterControl's complimentary monthly newsletter, GxP Lifeline, to learn more about the Corrective Action Software and the industry from feature articles, stories, best practice tips, and more.

Contact MasterControl Today for Information on Corrective Action Software Systems

Corrective Action Software System processes are central to any GxP system. MasterControl corrective action software ensures the corrective action or CAPA system improves product quality and safety, increases customer satisfaction, and ensures FDA compliance. To learn more about corrective action software contact MasterControl online or call toll free at 1.800.825.9117 to speak with a representative.


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