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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
Connect training to other quality processes and automate the routing, tracking, and follow-up of training tasks and even the grading of online exams.
The MasterControl CQMS manages all documents, tasks, processes, relationships, audits and training that must be administered and controlled throughout the clinical trial lifecycle.
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.
Bridges the traditional gaps that paper-based or disparate processes create between quality and manufacturing to drive immediate performance improvements and operational efficiencies.
MasterControl Supplier™ provides a single repository for maintaining all supplier quality data and documentation.