TMI-USA at INTERPHEX, New-York, April 16-18

Meet our Sales teams and learn more about our offer for Pharmaceutical industry processes validation:

  • A full range of autonomous data loggers measuring temperature, pressure and humidity for process validation in:
    • Steam sterilization
    • Ethylene oxide sterilization
    • Depyrogenation ovens
    • Freeze-drying
    • Climatic chambers
    • Sprays
    • Washing-disinfection
       
  • TMI-Orion Qlever validation software, for the acquisition, analysis, and visualization of the measured data.

Compliance with directives and norms:

FDA 21 CFR Part 11, EN 554, ISO 17665, EN 13060, EN 285, EN 868, EN ISO 15883, FD X 15-140/IEC 60068.3.11

Learn more about our offer for Pharma industry