Our design integrates the comprehensive recommendations of the Food and Drug industry norms and standards such as: EHEDG, 3A, GMP, ASME BPE and USP. The full automation of our Cleaning-In-Place units (with the exception of the lower cost Mobiclean series) ensures reliability and traceability of all operations, reproducibility of the CIP cycles and control of all cleaning parameters:
- Flow rate – pressure (mechanical action)
- Temperature (heating action)
- Contact time and detergent concentration (physio-chemical action)
- Conductivity of the final rinse, for example in accordance with USP standards
- These systems provide full traceability of the Operational steps using dedicated Audit-Trail and Batch Report modules utilizing a SQL database.