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CFR data loggers

Highly efficient validation of your sterilisation and freeze-drying processes.

CFR data logger for process validation and qualification

The challenge: Validating sterilization, freeze-drying, cleaning and disinfection processes

The validation of sterilization and freeze-drying processes as well as of cleaning and disinfecting equipment including the standard-compliant verification of successful process parameters in accordance with DIN EN ISO 285, DIN EN ISO 17665, DIN EN 13060, DIN EN ISO 15883 is legally required and forms a key element of quality assurance. However, this is only possible if the data loggers are positioned correctly during validation and the reproducibility of the measurement is guaranteed.

In order to ensure that operating procedures run seamlessly, the handling of the loggers, the validation process and the documentation must all proceed as efficiently and smoothly as possible. The same applies to calculation of the lethality, the holding phase and saturated steam conditions.

The testo 190 all-in-one solution supports you with innovative data loggers, intuitive software and practical accessories to meet these challenges. So you can always rest assured that the qualification and validation of sterilization, disinfection and freeze-drying processes will be carried out in an extremely efficient manner, in compliance with the standards.

The solution: The testo 190 CFR data logger system

The testo 190 system components

Data logger, multifunction case, CFR software and services

Data loggers

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Safe and reliable measurements: The data loggers

  • Robust: Tested for reliable operation from
    -50 to +140 °C during more than 1,500 operating hours

  • Simple: Battery replacement that is tool-free, safe and intuitive

  • Protected: Electronics in glass-metal bushing impervious to water

Multifunction case

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Configure and read out: The multifunctional case

  • Secure: Loggers transported in the built-in readout unit

  • Fast: Program and read out up to 8 data loggers in parallel

  • Error-free: Stable readout and programming

Intuitive operation: The CFR software

  • Guided: Preset, intuitive processes

  • Uncomplicated: Simple calculation of holding phase and lethality

  • Complete: Fast and comprehensive report generation

Supported working: The services

  • Complete: Realisation of validations & qualifications (DQ, IQ, OQ, PQ)

  • Tested: Accredited calibrations - also on site

  • Personal: Sterilization workshops by our experts

Which application interests you?

Freeze-drying

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Sterilization

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Cleaning and disinfection

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White paper

White paper

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White paper: testo 190 loggers in endurance testing

Test procedures and results on:

  • Robustness

  • Accuracy drift

  • Reliability of the battery

White paper

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White paper: Validation of steam sterilization

Expert knowledge on steam sterilization:

  • How it works and the risks involved

  • Regulatory requirements

  • Pharmaceutical safety and economic efficiency

Further downloads

Application example
Freeze-drying

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Application example
Sterilization

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Factsheet testo 190

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Product brochure testo 190

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