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CIP / SIP System

CIP / SIP System

Revolutionize Pharmaceutical Equipment Hygiene with Coralpt's CIP/SIP System

Coralpt Worldwide Pvt Ltd takes pride in introducing an advanced Cleaning In Place (CIP) and Sterilization In Place (SIP) system tailored for the pharmaceutical industry. Our cutting-edge solution is designed to elevate hygiene standards, ensuring the production of safe and sterile pharmaceutical products.

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Key Features:

  • Compliance with cGMP: The system is designed in accordance with Current Good Manufacturing Practices (cGMP), meeting and exceeding industry hygiene standards.

  • High-Quality Construction: All contact parts crafted from AISI 316/316L for durability and corrosion resistance. Non-contact parts made from AISI 304 to maintain hygiene standards.

  • Automated CIP Component: The CIP system utilizes a combination of chemicals, heated water, and other agents to clean pipes, storage tanks, and equipment involved in producing purified water or water for injection.

  • Effective Contaminant Removal: Target and eliminate contaminants such as proteins, nucleic acids, bacteria, viruses, fungi, yeasts, and endotoxins critical for maintaining product purity.

  • Versatile Cleaning Agents: Incorporates a range of specialized cleaning agents, including sodium hydroxide, nitric and phosphoric acids, peracetic acid (PAA), sodium hypochlorite, and chlorine dioxide.

  • Resource Optimization: Precisely controls flow rates, temperatures, and cleaning agent concentrations to optimize resource consumption, minimizing waste and reducing operational costs.

  • Automated Cleaning and Sterilization: Fully automated process eliminates the need for manual disassembly and reassembly of equipment, ensuring consistent and reliable results.

  • Customized Temperature and Pressure Control: Advanced temperature and pressure control mechanisms in the SIP component ensure effective sterilization while minimizing the risk of damage to sensitive components.

  • Monitoring and Validation: Comprehensive monitoring and validation features ensure the effectiveness of cleaning and sterilization processes through real-time data recording and validation protocols.

  • Ease of Integration: Designed for easy integration into existing pharmaceutical manufacturing setups, whether incorporating new equipment or retrofitting existing systems.

  • Enhanced Product Safety: Thorough cleaning and effective sterilization significantly reduce the risk of product contamination, ensuring the production of safe and sterile pharmaceutical products.

Coralpt's CIP/SIP system represents a commitment to delivering cutting-edge solutions that meet the evolving needs of the pharmaceutical industry. With a focus on efficiency, reliability, and compliance, our system sets a new standard for hygiene and product safety in pharmaceutical manufacturing operations. We look forward to discussing how our CIP/SIP system can enhance the efficiency and quality of your pharmaceutical manufacturing processes.