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.

Watch Videos

How MasterControl Makes Your Job Easier (3:50)
Creating a Paperless Process Using MasterControl (3:38)
Download Free Documents

White Paper: Does Your CAPA Need a CAPA?
White Paper: How to Kick-Start Your CAPA Process
White Paper: Simplifying CAPA: Seven Steps
White Paper: Foolproof Investigations: A Proven Approach for Root Cause Analysis in a Regulated Environment
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
Product Data Sheet: MasterControl CAPA MD™
Product Data Sheet: MasterControl CAPA Pharma™
Product Data Sheet: MasterControl CAPA™



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 software systems to meet best practice guidelines. The corrective action software systems from MasterControl ensures an accurate and reliable system for correction action or CAPA processes. It also ensures consistant 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 or 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

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 industry from feature articles, stories, best practice tips, and more.

Contact MasterControl Today

Corrective Action Software Systems (CAPA) processes are central to any GxP system. MasterControl corrective action software systems 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.


Related Links


Share This Article
Digg Technorati TwitThis del.icio.us Google Facebook StumbleUpon Yahoo! Buzz LinkedIn Slashdot MySpace Xing