In-Situ CIP-SIP System
CIP-SIP System
Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems are designed for automatic cleaning and disinfecting, ensuring seamless sanitization and sterilization. We specialize in designing, developing, manufacturing, supplying, and installing custom-made CIP and SIP systems. These modular, skidded systems are available in both automated and semi-automated models, tailored to the specific time cycles required for cleaning and sterilizing large, fixed, multi-tank systems.
As the pharmaceutical and biopharma industries evolve with increasing regulatory scrutiny, the demand for multiproduct manufacturing facilities continues to grow. This requires a precise and well-planned approach to ensure thorough cleaning and sterility of systems, and our solutions are engineered to meet these critical needs.
FACTORY ACCEPTANCE TEST (FAT) / SITE ACCEPTANCE TEST (SAT)
All our systems undergo rigorous testing in our dedicated FAT (Factory Acceptance Testing) area, fully equipped with all necessary utilities. We ensure that every instrument performs optimally under the specified conditions, providing reliable and efficient results.
Our quality assurance (QA) team meticulously oversees the entire process, ensuring that all required documentation is thoroughly prepared and maintained before and during the FAT/SAT (Site Acceptance Testing) phases. This attention to detail guarantees smooth validation and compliance, delivering systems that meet the highest industry standards.
ADVANTAGES
No Separate Installation Required
Custom Designed as per Product Flow
Heating/Cooling Options
Full/Semi-Automated Operation
Tailor-Made for Custom Requirements
KEY FEATURES
- Sanitary designed as per US FDA / cGMP / ASME compliance with ASME – BPE norms
- Contact parts: SS 316 L, mirror polished & electro polished
- All non-contact parts: SS 304 Matt finish
- Orbital tube welding
- Online acid, alkaline dosing provision
- SS 304 polished skid
- Sanitary moisture separator & pressure regulating valve
- Automation as per USFDA, 21 CFR part 11
- Cleaning validation with riboflavin test
- Bottom-mounted magnetic mixers with options for low/medium/high shear applications
- Flexible process parameters setting (Recipes)
- Sterile flange connections of top dish
- Load cell or Level sensors for weight measurement or level measurements
