Cleaning & Sanitisation process for manufacturing vessels and interconnecting process vessels is one of the most critical aspect to remove residues formed in vessel from the previous batches and to ensure contamination-free systems.
All valid pharmaceutical (e. g. USP, EP), technical rules and standards (e. g. DIN, ASME, GMP and FDA / ISPE Guidelines) are followed during the process. The CIP+SIP system is designed as package unit to perform CIP, SIP, and PHT processes.
Designed to perform Clean in place, Sterilisation in place, Pressure Hold test function for Mixing vessels, Filtration vessels and Holding vessels of different sizes in Life Science industry.
Clean in place, Sterilisation in place, Pressure Hold test function for Mixing vessels, Filtration vessels and Holding vessels of different sizes in Life Science industry.