Validation of your sterilization and freeze-drying processes with the CFR data logger system.

The Top 3 Advantages of the Product

Robust: Reliable operation from -50 ° C to +140 ° C during more than 1,500 operating hours


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


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

CFR data loggers for temperature and pressure control in process validation and qualification.

The validation of sterilization and freeze-drying processes as well as of cleaning and disinfecting equipment is a central element of your quality assurance and proves the high level of safety of your processed products. With the testo 190 CFR data logger system, which was specifically developed for use in the pharmaceutical industry, Testo supports you in meeting all regulatory requirements in a highly efficient manner. The CFR data loggers are available in four temperature and one pressure versions. They stand for robustness, durability and reliability. Leave your complete validation to Testo and benefit from a resource-saving full-service solution that ensures your GMP compliance. Alternatively, Testo is happy to support you with individual services specially tailored to your needs, such as training, calibrations, qualifications and validations. In any case, Testo is your reliable partner for meeting your individual requirements.

  • temperature measurement

  • freeze-drying

  • sterilisation

  • disinfection

  • data loggers

  • Cleaning technology

Target Industries
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