R&D and Production
Qualification and validation of processes
With the testo 190 CFR data loggers, which have been specifically developed for the pharmaceutical industry, you can validate your sterilisation and freeze-drying processes in a highly efficient and simple way.
Freeze-drying
- The testo 190 T3/T4 CFR temperature data logger monitors the temperature profile during freeze-drying processes in the pharmaceutical industry
- Qualification of the plate temperature with five measuring points per plate
- Steam in Place (SIP): Subsequent sterilisation of the system with superheated steam
Sterilisation
- The testo 190 T3/T4 CFR temperature data logger enables independent routine checks and validations of steam sterilisers
- Physical and biological evidence that the sterilisation method is suitable for the product
- Placement of the data logger’s probe tip in the core of the item being sterilised