Product Information

All of the product data sheets from our extensive product list.

  • MasterControl Enterprise Business Unit (EBU)™

    MasterControl Enterprise Business Unit (EBU)™

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  • Most Common Questions About the VxT

    Most Common Questions About the VxT

    MasterControl’s patented Validation Excellence Tool (VxT) is our answer to risk- based validation. We worked with former FDA officials and industry experts to develop the tool, which lets you leverage

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  • MasterControl eMDR™ Enhanced Forms

    MasterControl eMDR™ Enhanced Forms

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  • MasterControl Action Item™, Extension Request™ and Meeting Minutes™ Enhanced Forms

    MasterControl Action Item™, Extension Request™ and Meeting Minutes™ Enhanced Forms

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  • Is Chronic Paper Dependence Stifling Your Quality?

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  • Manufacturing Quality: Frictionless Quality and Compliance With eDHR

    Manufacturing Quality: Frictionless Quality and Compliance With eDHR

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  • MasterControl Integration Services

    MasterControl Integration Services

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  • MasterControl Dynamic Forms

    MasterControl Dynamic Forms

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  • MasterControl Professional Services

    MasterControl Professional Services

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  • MasterControl Implementation

    MasterControl Implementation

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  • MasterControl Integration Services

    MasterControl Integration Services

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  • MasterControl Training™

    MasterControl Training™

    Connect training to other quality processes and automate the routing, tracking, and follow-up of training tasks and even the grading of online exams.

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  • MasterControl Clinical Quality Management System (CQMS)™

    MasterControl Clinical Quality Management System (CQMS)™

    The MasterControl CQMS manages all documents, tasks, processes, relationships, audits and training that must be administered and controlled throughout the clinical trial lifecycle.

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  • MasterControl CAPA™

    MasterControl CAPA™

    Corrective and preventive action (CAPA) is the single-most critical element of any quality system, and must be managed as such to satisfy both FDA and ISO requirements.

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  • MasterControl Manufacturing Suite Silver™

    MasterControl Manufacturing Suite Silver™

    Bridges the traditional gaps that paper-based or disparate processes create between quality and manufacturing to drive immediate performance improvements and operational efficiencies.

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  • New ICH Q10 Harmonization Guidance for the Pharmaceutical Industry

    New ICH Q10 Harmonization Guidance for the Pharmaceutical Industry

    ICH Q10 is a guideline that describes a model approach for a modern pharmaceutical quality system.

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  • MasterControl Supplier

    MasterControl Supplier

    MasterControl Supplier™ provides a single repository for maintaining all supplier quality data and documentation.

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  • Guidelines For The European Medical Device Vigilance System

    Guidelines For The European Medical Device Vigilance System

    "How-to" information for medical device companies complying with regulations standardized by the MDDs (Medical Device Directives). Access the MEDDEV-5 when developing quality and compliance processes.

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  • FDA's Quality Systems Approach to Pharmaceutical CGMPs

    FDA's Quality Systems Approach to Pharmaceutical CGMPs

    Examine the FDA's Guidance for Industry Quality Systems Approach to Pharmaceutical CGMP Regulations and how MasterControl software can help modernize your quality system.

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  • MasterControl Corporate Brochure

    MasterControl Corporate Brochure

    Our customers are highly regulated companies whose goal is to create lifechanging products used by millions of people worldwide. Quality is critical to ensuring product safety and compliance.

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  • The Evolution of Validation Best Practices

    The Evolution of Validation Best Practices

    As practiced by many regulated companies today, software validation is the single most expensive and time-consuming aspect of automating or upgrading their quality management and compliance systems.

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