Easy to use and easy to learn, the Celsis Accel® system delivers results in just 18-24 hours for microbial limits (USP <61>) quality control testing and 4-6 days for sterility testing (USP <71>), allowing you to confirm more rapidly the quality of your products and quickly release them to market.

The ability of this rapid microbial detection system to confidently confirm the absence of contamination allows your in-house quality system to:

  • Shorten production cycle times
  • Decrease working capital requirements as well as safety stock
  • Reduce inventory requirements and warehouse space costs
  • Receive earlier notification in the event of a contamination
  • Respond to contamination and conduct investigations faster

How it Works
The Celsis® assay rapidly confirms the presence or absence of microbial contamination using an amplified ATP-based bioluminescence reaction. Our method preserves your originally validated sample preparation methods, such as bioburden filtration or direct inoculation. Once prepared, the samples are enriched for a period based on your product specification. Once completed, samples require minimal steps before being loaded into the Celsis Accel®. Up to four variable-volume reagent injectors ensure accuracy, reduce sample handling and increase flexibility. System throughput runs as high as 30 tests per hour with the option of simultaneously combining multiple batches or protocols into a single run. The user interface of the LIMS-compatible system software objectively interprets and displays results in a color-coded table or graphical view.

Enzyme Technology: How Amplifying the ATP Bioluminescence Reaction Produces Faster Time to Results

    • Enhanced system and data security
    • Remote user access software for accessing or monitoring results from multiple locations
    • Comprehensive data analysis and trend reporting
    • Developed exclusively for industrial microbiology laboratories
    • Click to start: enjoy walk-away automation
    • Offline incubation maximizes system throughput
    • Customizable security levels
    • Runs up to 30 tests per hour
    • Product validations for use of the Celsis® system have been approved by regulatory agencies worldwide
    • Allows full compliance with the FDA’s 21 CFR Part 11 and the European Union’s Annex 11
    • Fully validated on current Microsoft® Windows® operating systems
    • Automated data capture and storage, exporting to common database programs, including Excel and Access
    • Small-scale footprint: width x height x depth / 13 x 14.5 x 20.5 in / 33 x 37 x 52 cm