CIP/SIP Systems

CIP/SIP Systems
  • CIP/SIP Systems

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    Pharmatec CIP/SIP Systems are designed for purification and sterilization of pharmaceutical units, systems and single components. The modular design of these systems and the use of approved standard components of qualified suppliers guarantee efficient and innovative project handling within a short time. The system design guarantees simple self-purification. CIP Systems can also be carried out inline-sterilizable (SIP). Use of special dosage and heating/cooling systems provides a constant and consistent high purification quality. All valid pharmaceutical (e. g. USP, EP) and technical rules and standards (e. g. DIN, ASME, GMP and FDA / ISPE Guidelines) are followed and applied.BenefitsStandard structured data-based project management Unitized process systems for different quantities Adaptable to specific room conditions due to flexible construction regarding design and floor plan Concept development of all necessary steps by use of pre-tested software modules to secure high process balance CIP/SIP design according to the latest GMP requirements Product contiguous parts standard of stainless steel 1.4404/ 1.4435 (AISI 316L) Use of control components from Siemens, Allen Bradley, Mitsubishi and others Simple handling by self-explanatory menu navigation Highest possible safety for product and user by permanent process monitoring FAT on manufacturer plant with all necessary process media as well as commissioning and qualification activities (IQ / OQ, i. a. PQ support, SAT) at customer site and data-based creation of system and qualification documentation
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