99 % certainty is not enough.
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.
Integrated system comprising sensors, software and services
Seamless recording and documentation of all audit-relevant IAQ (Indoor Air Quality) 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.
Download the comparison brochure now.
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.
Find out more about the measuring solutions that can support you in your laboratory and cleanroom processes and in pharmaceutical logistics.