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Email :PharmaSources@imsinoexpo.com
Whatsapp :+86-13621645194
Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East,Africa
Sample Provided: no
CIP cleaning system will prepare cleaning solution automatically by setting program (program can be set via window), pneumatic control valve, transfer pump and reflux pump enables cleaning solution transfer, return circulation cleaning, drainage and recycle. The on-line conductivity meter, PLC and touch screen realize automatic monitoring and control. CIP system can be designed in movable and fixed type, and also can be designed in the way of single and multiple tanks.
System configuration:
Cleaning tank
Heat exchanger
Transfer pump
Reflux pump
Temperature meter
Pressure gauge
Conductivity meter
Level meter
PH meter
Control system
Pipe accessories
Validation documents: DQ,IQ,OQ,PQ
Working process:
CIP cleaning system will prepare cleaning solution automatically by setting program (program can be set via window), pneumatic control valve, transfer pump and reflux pump enables cleaning solution transfer, return circulation cleaning, drainage and recycle. The on-line conductivity meter, PLC and touch screen realize automatic monitoring and control. CIP system can be designed in movable and fixed type, and also can be designed in the way of single and multiple tanks.
Technical characteristics:
Compact structure, limited space needed, package device is easy for operation and maintenance on site, and connect with existing equipment.
Support multiple module extension (Hardware, software), automatic control, easy to connect with other device
Equipped with on-line cleaning and sanitization port.
Separate preparation, no pollution happened to production site
It is convenient and effective for the tanks, pipes and other production equipment on site, and the cleaning process is carried out in a sealed tank and pipes without cross-contamination.
Online monitoring of critical process parameters, complete data collection and data output
Complete FAT, SAT and validation documents, meet verification standard of management organization.
Meet validation requirements of SFADA, USA FDA and EU EMEA, and ASME-BPE standard.
To improve and optimize production capacity.
To improve cleaning efficiency.
To avoid any risk during operation and save labor cost.
To save cost for detergent、steam、water and production cost.