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.
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.
Holistic system consisting of sensors, software and services
Seamless recording and documentation of all audit-relevant climate parameters in pharmaceutical production
Compliant with GxP and 21 CFR Part 11
This GxP Dictionary explains the majority of terms relating to GxP, qualification, validation and quality assurance.
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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.
Find out more about the measuring solutions that can support you in your laboratory and cleanroom processes and in pharmaceutical logistics.