Clean-in-Place (CIP) & Wash-in-Place (WIP) Systems
Our CIP/WIP Skids are engineered to provide reliable, fully-automated cleaning and sanitization for process equipment and piping. By eliminating the need for manual dismantling, these systems ensure a repeatable, validated cleaning process that minimizes downtime, maximizes water efficiency, and upholds the highest standards of purity in Pharmaceutical, API, and Biotech facilities.
Core Engineering & Performance
Every GR Pharma Machine CIP system is custom-designed to suit the specific layout and cleaning requirements of your plant, emphasizing both sustainability and efficacy.
Automated Cycle Control: Features a PLC-based control system with recipe management, allowing for precise control over rinse times, detergent concentrations, and temperatures.
Sanitization Excellence: Specialized cycles for circulating purified water, hot water, or chemical detergents, followed by air-blowing or steaming to ensure a sterile environment.
Optimized Fluid Dynamics: Designed to maintain the necessary turbulent flow and spray ball pressure required to remove even the most stubborn residues from vessels and complex piping.
Sustainability: Includes optional recovery tanks for the reuse of final rinse water in the initial rinse of the next cycle, significantly reducing water and chemical consumption.
Key Features
Mobile & Stationary Options: Available as compact, trolley-mounted mobile units for versatile use across the facility, or as large-scale stationary multi-tank systems.
Sanitary Instrumentation: Equipped with high-precision conductivity sensors, flow meters, and temperature transmitters to monitor and record every phase of the cleaning cycle.
Hygienic Construction: Fabricated entirely from AISI SS 316L for contact surfaces, utilizing orbital welding and high-purity valves to ensure no “dead legs” where bacteria could grow.
Heat Exchange Integration: Optional shell-and-tube or plate heat exchangers for rapid heating of cleaning media.
Operational Benefits
Validated Cleaning: Provides the consistent, data-logged performance required to comply with FDA and cGMP cleaning validation protocols.
Reduced Human Exposure: Minimizes operator contact with hazardous chemicals and high-temperature water.
Zero Cross-Contamination: Ensures that complex equipment like High Shear Mixers and Fluid Bed Dryers are thoroughly cleaned between product changeovers.
21 CFR Part 11 Compliance: Advanced automation options include secure data logging and electronic signatures for batch report generation.
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Serving Customers
Application Areas
The GR CIP/WIP systems are essential for the high-purity cleaning of:
High Shear Mixer Granulators (HSMG)
Fluid Bed Dryers (FBD)
Reaction Vessels and Fermenters
Interconnecting Process Piping
Blending Bins and Storage Tanks
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