Validator 2000
Thermal validation solution for inspection of pharmaceutical, biotechnology and medical device manufacturing
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For nearly two decades the Kaye Validator 2000 has been the standard for wired Validations systems in the Pharma/ Biotech industry. Thousands of users trust and rely on the accuracy, reliability and proven performance of the Validator 2000. With the introduction of the new Validator AVS, Kaye wants to ensure our large installed base of existing Validator 2000 users that, as we have done throughout our history, we continue to provide support and allow them ample time to properly plan for their future and provide uninterrupted validations.
Our support teams are providing flexible solutions for any customized requirements for users owning a Validator2000® unit, and supporting them through the transition to the Kaye Validator AVS.
• Intuitive study setup and extensive process calculations simplify valdiation process
• Improved data analysis, including ability to graph and report unlimited cycles and up to 25 groups
• Centralized network management of all passwords and audit trails
• Ability to merge data files from multiple Kaye Validator and ValProbe studies
• Sensor input modules minimize sensor handling and calibration, including 4/20 mA inputs
• Fully automated sensor calibration
• Operates standalone or with PC
• Enables compliance with FDA 21CFR Part 11 guidelines
• Total system accuracy, following guidelines for uncertainty measurement of 0.17°C (k=2)
• Steam Sterilizers (Autoclaves)
• Dry Heat Sterilizers
• Steam in Place (SIP)
• Water Cascade/Fall Sterilizers
• Incubators
• Stability Chambers
• Freezers
• Freeze Dryer/Lyophilisation
• Vessel
