Elevating Aseptic Processes in Pharma Manufacturing
Pharmaceutical manufacturing necessitates stringent sterility measures and precision in decontamination. CURIS responds to these needs with advanced Hydrogen Peroxide (HHP™/ hybrid hydrogen peroxide) 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, optimizes isolator controls, and enhances pass-through and airlock functionality. Experience enhanced regulatory compliance and steadfast commitment to quality 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.