Measuring instruments and all-in-one solutions for pharmaceutical production
If pharmaceuticals are produced and stored under the wrong climatic conditions, the stability and therefore the efficacy of the drugs can suffer as a result. Possible consequences: commercial losses or even extensive compensation claims.
Don’t let it come to that: Testo can support you in a GMP-regulated environment with reliable measuring technology and all-in-one solutions that are audit-safe.
IAQ monitoring: Stationary monitoring of environmental parameters
From simple hygrometers and data loggers through to automated IAQ monitoring systems: Testo’s measurement solutions offer you reliable and continuous measurement of the relevant ambient conditions. This enables you to reliably comply with external and internal quality requirements in GMP-regulated environments.
The all-in-one solution: The testo Saveris Pharma environmental monitoring system
Uninterrupted monitoring during pharmaceutical production – using one system
Integrated system comprising sensors, software and services
Seamless recording and documentation of all audit-relevant IAQ parameters in pharmaceutical production
With the testo 190 CFR data loggers, which have been specifically developed for the pharmaceutical industry, you can validate your sterilization and freeze-drying processes in a highly efficient and simple way.
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 sterilization of the system with superheated steam