MasterControl specializes in quality management software for regulated life science companies and laboratories. MasterControl's QMS software automates and integrates quality processes and helps ensure the stability of CLIA quality control in regulated environments. In fact, MasterControl's QMS software solution was selected as the FDA's QMS software solution of choice.
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With MasterControl QMS software, meeting CLIA quality control requirements becomes a series of comfortably automated processes. For example, when a company utilizes MasterControl's QMS system - customer complaints, full-scale document control/management, change control, audit control, nonconformance management - deviations and CAPA processes are all streamlined, automated and integrated for complete CLIA quality control and compliance with FDA regulations and ISO standards.
MasterControl automates the routing, approval, escalation, delivery and archival of all quality-related documentation including all documentation required for CLIA quality control compliance. MasterControl also automates the delivery of training tasks and the approval and follow-up of complete or incomplete training assignments. Clinical management training assignments and exams can be configured to trigger the release of CLIA-related documentation when and only when essential training is complete and the document in question can "legally" be released. MasterControl also streamlines complaint handling and automatically processes high-priority complaints via one of MasterControl's sophisticated CAPA control solutions.
The list of benefits that MasterControl software can provide for laboratories striving to conform with CLIA quality control requirements is certainly a long one.
Learn more about automating CLIA quality control by contacting a MasterControl representative.