Compliance management reporting is required during audit procedures (e.g. FDA, ISO or CLIA audits, etc.) and for internal quality checks. Compliance reporting may entail deviations, change control, documentation or CAPA analysis in addition to a host of additional quality related tasks and processes.
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MasterControl provides web-based solutions that streamline processes associated with total quality management and compliance management reporting.
MasterControl contributes to highly regulated environments and business intelligence by providing compliance management reporting solutions for GxP process management, quality audits and document control. MasterControl also offers specialized solutions for the pharmaceutical and medical device industries.
Since MasterControl implements a flexible business model, it can continually provide a cost of acquisition, implementation and validation that can be significantly lower than the competition.
To access a wealth of additional MasterControl compliance management reporting information including white papers, customer videos, webinars, product data sheets, online demonstrations, etc. please visit the MasterControl Resource Center.
For more information in regard to streamlined quality management and compliance management reporting, please feel free to contact a MasterControl representative.