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SCANRDI®

Bring Your Sterility Testing to the Next Level

SCANRDI® revolutionized rapid microbial detection when it was first introduced and its speed and sensitivity continue to answer market needs today.

Its unique technology delivers actionable sterility results in 4 hours or less, so you know you can continue with production or if you need to take action immediately.

When You Need to Know Now

SCANRDI® enables same-shift detection of microbial contaminants in filterable drug products. The US Food and Drug Administration (FDA), European Medicines Agency (EMA), and other regulatory bodies support the use of validated Rapid Microbiological Methods (RMM) for sterile product release - especially in the case of shelf-life products, where a rapid result is more suitable than a compendial 14-day test.

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Enhanced Device Functionality

NEW! Combine your SCANRDI® instrument with SCANFILTERTM, our new filtration device.

  • Enhanced user-friendliness, encompassing streamlined handling, optimal sample visibility, and effortless packaging access
  • Improved robustness with high-quality materials to minimize operator errors
  • Enhanced user experience facilitated by the device, necessitating minimal manipulation with heightened precision
  • Enhanced device functionality leads to increased workflow efficiency and reduced error risk

Improve Productivity and Compliance

Increase Your Market Competitiveness

  • Safely release your short shelf-life & generic products faster
  • Optimize your distribution logistics with just-in-time inventory management of stock and choose your most affordable shipping option

Control Your Manufacturing Process

  • Rapid in-process, bioburden and sterility results give you confidence that your production is operating properly
  • Facilitate your investigation process to quickly return to normal operations
  • Eliminate lab bottlenecks

Be Confident in Your Compliance

  • Ensure your electronic compliance with 21 CFR part 11 enabled software, barcode scanning traceability, several approval levels and a full audit trail
  • Feel reassured in your validation process with support from bioMérieux including URS completion guide, IOQ guide, primary validation guide, suitability guide and Drug Master File (DMF)