Monitoring, Alarming, Reporting & Validation System
For Demanding Pharma/Biotechnical Applications

• Precision validatable monitoring, recording & reporting system for temperature and temperature & humidity can be used for enterprise-wide monitoring or standalone mapping;
  
  
• High-accuracy digital recording of time-based temperature and relative humidity requires no wiring, special probes, or lengthy setup;
  
  
• For validation applications, high stability sensors with no wiring errors eliminate the need for costly pre-cal and post-cal checks;
  
  
• Create validatable reports or any test period. Tamper-proof data loggers and encrypted electronic records meet FDA requirements for 21 CFR Part 11.
  
  
• Battery-powered data loggers with 10-year life offer quick and flexible deployment

Veriteq's system provides an easy-to-use and cost-effective method for validating temperature and humidity-sensitive equipment, systems, and processes in FDA / GMP pharmaceutical environments.

Designed for demanding pharmaceutical applications, Veriteq's solutions provide a powerful and easy-to-deploy alternative to thermocouple-based equipment and bulky data acquisition systems.

The Veriteq VL-series datalogging system is comprised of one or more VL-series validatable dataloggers and the Veriteq vLog software package.

VL-series dataloggers include the VL-1000 Temperature Logger, the VL-2000 Relative Humidity and Temperature Logger, and the new VL-1000-VLT Very Low Temperature (to -86° C) Logger.

Applications:

• Ambient Temperature and Humidity monitoring of Labs
• Warehouse environment studies
• Stability chamber qualifications
• Clean room monitoring
• Pharmaceutical cold chain validation (shipping containers, processes, temporary storage areas, etc.)
• Storage and holding rooms
• Cold rooms
• Freezers and Refrigerators

For more information, please email a Veriteq representative or contact us online.

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