CIP Systems (Clean In Place)
CIP systems allow for automatic, reproducible, and verifiable cleaning of equipment and process circuits without requiring disassembly. They are designed to ensure the highest standards of hygiene and product safety, reducing manual intervention and ensuring stability in critical cleaning parameters.
CIP Systems (Clean In Place)
CIP systems allow for automatic, reproducible, and verifiable cleaning of equipment and process circuits without requiring disassembly. They are designed to ensure the highest standards of hygiene and product safety, reducing manual intervention and ensuring stability in critical cleaning parameters.
They are custom configured based on the type of installation, product, and regulatory requirements, facilitating qualification and validation processes in GMP environments.
Technology and design
Productive versatility
CIP of reactors
Hose cleaning
CIP for process lines
Fixed CIP System Configuration
Permanently installed on-site, directly connected to process equipment and networks. It is designed for facilities with high cleaning frequency and allows for full integration with automation systems and dedicated utilities, ensuring maximum stability and traceability.
Mobile CIP System Configuration
Mounted on a skid for easy movement to service different equipment within the plant. Maintains the same automatic process controls, providing operational flexibility when a permanent installation is not required.
Solutions and benefits
Automatic cleaning without equipment disassembly
They allow cleaning equipment and entire lines without manual intervention or disassembly.
Cleanliness cycle repeatability
Automatic control ensures that each cycle always runs under the same conditions.
Reduction of cross-contamination risk
Controlled cleaning between batches prevents product carryover in facilities multi-product.
Complete control of critical cleaning parameters
They allow monitoring flow rate, temperature, conductivity, and time throughout the entire cycle.
Adaptation of the system to the existing installation
They are dimensioned according to line length, number of equipment, and product characteristics.
Ease of validation in GMP environments
Parameter logging allows for the documentation and validation of cleaning cycles.