Integrated environmental monitoring for pharma

In pharmaceutical manufacturing and clinical environments, such as cleanrooms, operating theatres or filling systems, the need to monitor humidity levels and temperature is essential

Shortcomings in the correct management of these environments can result in product degradation and failure to adhere to 21 CFR Part 11.

Testo now offers pharmaceutical companies a complete solution for the management of clinical environments, with instruments for continuous monitoring, data logging to 21 CFR Part 11 standard, and spot checking of key parameters.

Differential pressure transmitters - for continuous measurement and control of pressure between rooms or zones.

Hygrotest humidity transmitters - to provide precise and reliable monitoring of temperature and humidity and calculation of variables such as dew point and absolute humidity.

Data loggers - non-volatile memory loggers for secure long-term recording of data to comply with 21 CFR Part 11.

Reference measuring instrument - for precision spot checks to back-up transmitters and loggers, quick indication of drift and environmental change and on-site calibration/verification of instruments (via direct connection).

In addition it can offer Ukas calibration of instruments, to ensure their ongoing accuracy and compliance.

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