Elevating Aseptic Processes in Pharma Manufacturing
Pharmaceutical manufacturing necessitates stringent sterility measures and precision in biodecontamination. CURIS responds to these needs with advanced Hybrid Hydrogen Peroxide Technology (HHP™) decontamination systems, effectively targeting contaminants in crucial areas like production spaces, isolators, pass-throughs, and airlocks, bolstering your pharma process sterility.
Tailored Biodecontamination for Optimizing Pharma Operations
CURIS' 7% vaporous hydrogen peroxide technology offers meticulous control in pharmaceutical manufacturing, aiding sterility from API handling to final product packaging. Our systems bolster efficiency, optimize isolator controls, and enhance pass-through and airlock functionality. Experience enhanced regulatory compliance and steadfast commitment to quality contamination control with CURIS.
Decontamination Solutions for:
Sterility Assurance Testing | Production & Fill Line | Cleanrooms
Sterility Assurance Testing
Sterility assurance testing is critical for quality assurance in pharmaceutical industries. It requires an impeccably controlled environment with exacting biodecontamination methods. CURIS system contributes to this vital process with tailored solutions for isolators or cleanrooms, ensuring sterility testing accuracy.
Cleanrooms: Pass-throughs and Airlocks
Maintaining cleanroom integrity depends on the proficient management of pass-throughs, airlocks, and cleanrooms themselves. CURIS' decontamination systems for automated pharmaceutical manufacturing offer potential cost savings and support stringent cleanroom controls for enhanced efficiency, all with validatable, repeatable results.
Production and Fill line
Aseptic production and fill lines demand rigorous environmental controls to mitigate risk. CURIS's advanced decontamination systems uphold these standards, especially within restricted-access barrier systems (RABS). Our solutions aim to prevent potential contamination events, promoting operational efficiency and patient safety.
CURIS Applications
Room & RABS Decontamination
Engineered for comprehensive room decontamination, the CURIS 3 system is designed to enhance your facility’s safety and compliance standards, helping you to maintain sterility in your pharmaceutical manufacturing processes.Learn More
BSC & Filter Housing Decontamination
Specifically tailored for pharmaceutical manufacturing, TRINITY provides a modular solution for BSC & filter housing decontamination. It supports product integrity and aseptic conditions throughout your manufacturing journey.Learn More
Integrated Isolator Decontamination
The 7000ei system is designed for the unique challenges of pharmaceutical production. It offers reliable decontamination while preserving closed, sterile environments that are critical for quality and safety in the production process.Learn More
Passthrough, Chamber, & Enclosures
CURIS Custom Facility Integration
Custom Facility Integration safeguards a single room or your entire facility. Crafted for integrating rooms and facilities, it ensures thorough decontamination, maintaining an aseptic environment crucial for pharmaceutical manufacturing.
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Decontamination & Validation
CURIS Services assist in enhancing your facility’s safety and compliance. Offering everything from decontamination services to Installation, Operational, Performance Qualification (IOQ/PQ), and Preventive Maintenance (PM), our team enables you to focus on what matters most – delivering quality pharmaceuticals to the market.Learn More
Data Compliance
Streamline your pharmaceutical decontamination processes with CSDM. Our cloud-based, data compliance system handles automated decon jobs, data logging, report generation, and more. This all while ensuring seamless and traceable decontamination practices in line with regulatory requirements.Learn More