MasterControl Documents™
Automates the entire lifecycle of all documents-based processes, including task assignment/routing, follow-up, tracking, escalation, review, and document approval.
MasterControl Training™
Automates the assignment and monitoring of training tasks and the grading of online exams to ensure compliance with FDA cGMP. It automatically sequences all training courses, so that, after a prerequisite course is completed, the next one is launched. The software also provides a group sign-off feature for verifying the training of large groups of employees. Training management can be integrated with the rest of the quality system, so that any change to a document or process that warrants new training will automatically invoke training tasks upon approval of the change.
MasterControl CAPA™
Connects with various quality subsystems to track incidents, starting with problem identification and analysis, proceeding, when warranted, to corrective action (CAPA). A CAPA can automatically be launched from another form, with the software automatically entering all relevant data to ensure compliance with FDA cGMP.
MasterControl Change Control™
Streamlines the change control procedure for faster turnaround. It offers a best practice form that incorporates the latest requirements for FDA cGMP, GCP, and GLP.
MasterControl Nonconformance™
Is designed to automate, manage, and streamline the process for identifying, evaluating, reviewing, and handling of any nonconforming materials and finished products to ensure compliance with the guidelines of FDA cGMP.
