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Comprehensive Standard Package
Statistical methods for analysis of process deviations based on sample data acquisition. Typically for net content control of prepacked products.
Seamless and traceable documentation of the production and fill process. Guided operation at the Testplace for efficient data acquisition.
Complies with stringent requirements of the pharmaceutical industry. Ready for US FDA 21 CFR Part 11 compliant operation.
|●||Networked SQC/SPC system; Modular expandable; Centralized database; 3 concurrent clients included; Online monitoring and alarms; Standard reports included|