SteraMist BIT is Fully Validated to Comply with Good Manufacturing Practices (cGMP) and Good Laboratory Practice (cGLP) Environments
A TOMI technician is available to work through many decontamination validation processes. Validate a 6-log kill with one or more of the following methods TOMI has to offer!
TOMI’s experts can assist in every step, from a simple validation technique to a Pharmaceutical’s Qualification: requirement of Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ).
TOMI recommends the efficacy of the SteraMist technology to be empirically tested using Chemical Indicators (CIs), Biological Indicators (BIs), and/or Enzyme Indicators (EIs) to ensure a 6-log kill.