Product description

Pharmaceutical manufacturing process equipment are generally cleaned using a strategic CIP system design that meets ASME-BPE standards; CIP plays an vital role in optimizing the cleaning and validation processes Designing a CIP system begins by sizing for sufficient flow and pressure to thoroughly remove residue, reduce cycle times, and rinse effectively. Clean-in-Place (CIP) Systems are either manual or automated for cleaning the interior surface of process lines & vessels, tanks mixers, blenders, homogenizers etc., without dismantling the equipment. Thorough, repeatable in-place cleaning is mandatory as per cGMP and critical to the quality of product. CIP Systems are available in from Tank to Multi Tank or dual operating, custom built and engineered, both in flameproof and non-flameproof.
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Specifications

Categories Laboratory and Analytical EquipmentCleaning Equipment; Pharmaceutical Machinery & TechnologyEngineering; Pharmaceutical Machinery & TechnologyQuality control
Sales markets Western Europe; Eastern Europe; Middle East; Asia; Australia; North America; Africa; Central/South America
Supplied from India
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CIP System

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