Safeguard Your Production: Guaranteed Sterility with Pharmatech Process Steam In Place (SIP) Equipment

Experience the efficiency and reliability of our customized Steam-in-Place (SIP) solutions

SIP

In the fast-paced world of pharmaceuticals, food, and beverage production, maintaining sterility is paramount. Here at Pharmatech Process, we understand the critical role Steam in Place (SIP) systems play in achieving this goal. SIP, a widely adopted sterilization method across various industries, utilizes thermal energy from steam to eliminate microorganisms within processing equipment.

Our expertise extends beyond SIP systems – we offer comprehensive Cleaning-in-Place (CIP) solutions as well. Together, CIP and SIP form a powerful duo, ensuring a completely automated cleaning and disinfection process, eliminating the need for time-consuming disassembly and reassembly. This translates to efficient production cycles and minimizes risk of contamination between batches.

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SIP Guidelines for Sterile Processes

Prepare for SIP

Clean thoroughly (CIP) to remove soils. Verify steam supply for optimal sterilization.

Introduce Steam Strategically

Inject high-quality steam at the highest point, purging air through monitored drains.

Ensure Complete Steam Coverage

Utilize low-point trap valves with sensors to monitor and achieve uniform temperature.

Eliminate Air Pockets

Employ monitored high-point bleeds to meticulously remove air for effective sterilization.

Optimize Flow Path

Avoid parallel paths during air removal. Maintain flow direction for efficient drainage (minimize hoses, dead ends).

Hold at Temperature

After steam introduction, include a hold time to ensure all components reach the target temperature.

Maintain Active Steam Flow

Throughout the hold, maintain steam flow to guarantee successful sterilization.

Protect Sterile Process Boundary

As condensate drains, implement measures to prevent contamination.

Boost Production Efficiency: Download Our Steam In Place (SIP) Equipment Guide!

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Features

Complete exposure to steam for all surfaces
Ability to withstand the pressure that is generated by the sterilized steam
Ensuring complete elimination of entrapped air or non-condensable gases with the help of adequately designed air vents and retentive filters
Ensuring complete elimination of entrapped air or non-condensable gases with the help of adequately designed air vents and retentive filters
Provisions to cool the vessel after the process
Properly recording, monitoring, and maintaining the temperature at critical points

Our Benefits

Increased levels of sterility assurance and product safety

Reducing the need for multiple aseptic connectors

Integration with CIP

Reducing multiple sources of possible contamination

Customization options for different sizes and volumes

Reduced Labor Costs

Why Choose Pharmatech Processs?

Reliable Performance

Pharmatech Process prioritizes quality and reliability. Our equipment is built to withstand rigorous use and deliver consistent, effective sterilization cycles.

Validation and Support

We offer validation support to ensure your Steam In Place (SIP) system meets regulatory requirements. Our dedicated team is available to provide ongoing support and maintenance.

Commitment to Safety

Safety is paramount at Pharmatech Process. We prioritize features that protect personnel and ensure a contamination-free environment.