Meet our Sales teams and learn more about our offer for Pharmaceutical industry processes validation:
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A full range of autonomous data loggers measuring temperature, pressure and humidity for process validation in:
- Steam sterilization autoclaves
- Ethylene oxide sterilization autoclaves
- Depyrogenation ovens
- Freeze-dryers
- Climatic chambers
- Low temperature freezers
- Sprays
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Washers
- TMI-Orion Qlever validation software, to create and generate specific validation reports, compliant with FDA 21 CFR Part 11, FDX 15-140/IEC 60068.3.11, EN 554, ISO 17665, EN ISO 15883 requirements
