cGMP Standard Single Use CIP/WIP System |
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In today's pharmaceutical processes, proper CIP integration is critical to the overall success of the operation. CIP integration starts with the proper selection of the CIP System Skid to deliver the required cleaning parameters to the intended targets. The variables of temperature, velocity/pressure, chemical concentration, and exposure time are precisely controlled by the Niro Pharma Systems CIP System Skid, which can be configured with many options not only to deliver the specified CIP parameters, but to do so in a reliable, repeatable and verifiable manner.
Niro Pharma Systems CIP / WIP System Skids are completely designed, engineered, fabricated, automated and tested in our Hudson, Wisconsin workshop. This vertically integrated approach allows for open communications between disciplines, thus improving response time to any variances that may occur during the project life-cycle. A qualified Niro Project / Process Engineer is assigned to your project to facilitate discussions regarding site-specific requirements, integration concerns, and final FAT protocols. Defining and configuring the final CIP System Skid is not the only key to success in the integration of CIP into your hygienic process. Niro Pharma Systems can further assist you in the proper integration techniques of the CIP System Skid into your operating plant, ranging from conventional "make / break" manual flow-panel methodology to the latest in matrix piping technology that utilizes mix-proof valve systems. Technical DataSingle use CIP / WIP System Skid
OptionsNiro Pharma Systems Standard, Single use CIP System Skid can be configured with the following options to meet your specific needs.
Dimensional Information
Standard Documentation Package
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