When testing the stability of drugs according to the recommendations of ICH (International Conference on Harmonization) products must be stored under defined climatic conditions.
These test chamber series VP were specially developed for use in laboratories according to ICH guidelines.
Test space volumes: 600, 1300 and 2000 l
Temperature range: +10 °C to +50 °C
Humidity range: 20 % to 90 % RH
The documentation of temperature and humidity is obtainable via an interface and our optional software S!MPATI* Pharma (in accordance with FDA 21 CFR, Part 11) and also possible via an independent measurement system.
Qualification documentation according to FDA requirements is available.
Leaflet Stability Testing GMP & FDA (pdf)