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Corrective Action Plan
MasterControl offers a line of regulatory compliance products, including a corrective action plan to address different levels of quality and compliance.
FDA and EU regulated companies need to implement a CAPA processing system in order to comply with industry best practices. MasterControl offers a line of regulatory compliance products, including a CAPA software and a corrective action plan to address different levels of compliance.
About MasterControl Inc.
MasterControl Inc. has been a global provider of GxP process management software helping regulated companies attain and sustain regulatory compliance year after year. MasterControl suite is easy to deploy, easy to validate, and easy to maintain by incorporating an industry best practice corrective action plan with the latest software solutions
Implementing a Compliant Corrective Action Plan
For FDA regulated manufacturers, implementing a corrective action plan is essential to guaranteeing regulatory compliance. MasterControl's corrective action plan system offers an integrated, easy to use approach to compliance by connected the CAPA process with change control, training, and other quality systems. MasterControl CAPA™ includes the following features:
- Corrective action plan best-practice forms
- Connected quality processes
- Web-based system that allows customers, vendors, and others outside the company to submit a customer complaint or product issue report
- Integrated with the training application
- Advanced analytics and reporting
For More Information
Experience easier regulatory compliance, faster software validation, and better process management with MasterControl's GxP Process Management Software which includes a CAPA system and a corrective action plan. MasterControl's Resource Center is a comprehensive site that offers all of the educational and research materials FDA regulated companies need to succeed with a complete corrective action plan. These resources include:
Questions? Contact MasterControl Today
To learn more about MasterControl's CAPA software and corrective action plan contact MasterControl online or call toll free at 1.800.825.9117 to speak with a representative.
Related Items:
- Corrective Action Request
- Document Version Control
- GMP Facility
- GMP Guidelines
- GMP Regulation
- Internal Audit Reporting
- Market Regulated
- Serious Adverse Event
- Assurance Quality Tool
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Call us for a free consultation:
800-825-9117
 
Why is MasterControl the Right Software Solution for Your Industry?
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Compliant.
Sustained Regulatory
Compliance

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Connected.
Integrated Quality
Management

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Complete.
Enterprise-wide
Product Application

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Learn More
 
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