Pharmaceutical Production
Improper climatic conditions during production and storage can compromise the stability and efficacy of pharmaceuticals. Avoid these risks with Testo’s reliable measurement technology and all-in-one, audit-safe solutions, designed to support your operations in a GMP-regulated environment.
From basic hygrometers and data loggers to advanced automated IAQ monitoring systems, Testo provides reliable measurement solutions for continuous monitoring of essential ambient conditions. Our technology ensures consistent compliance with both internal and external quality standards 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 provides clear explanations for the majority of terms related 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.