Skip to Content
HomeProductsIndustrial MicrobiologySterility Testing Consumables, Media, Instruments and Software

Sterility Testing Consumables, Media, Instruments and Software

Sterility testing is a critical quality control requirement for GMP-manufactured products purporting to be sterile. False negative results risk releasing contaminated products, while false positives trigger lengthy and costly investigations. As regulatory expectations evolve — from pharmacopoeial compliance to digital data integrity — confidence in your sterility test results depends on more than just the test itself. Our comprehensive portfolio of sterility testing solutions is designed to meet the full spectrum of regulatory requirements, including USP <71>, the European Pharmacopoeia (Ph. Eur. 2.6.1), and the Japanese Pharmacopoeia, while supporting your laboratory's digital transformation.

Regulatory expectations around data governance have expanded significantly — QC laboratory data, including sterility testing records, is now firmly in scope of 21 CFR Part 11, EU Annex 11, and broader data integrity frameworks and subject to good document practices (ALCOA++).

Beyond data integrity, speed is increasingly critical. For short shelf-life products such as cell and gene therapies, release decisions cannot wait for the full 14-day compendial sterility test. Rapid Microbiological Methods (RMMs) based on proven technologies such as ATP bioluminescence are gaining broad regulatory acceptance, most notably with the recent introduction of USP <73>, which became effective August 2025.


Products

Products







Operator cutting the tube of the Sterility Testing Steritest device with the Velax cutting clamp

Built on 50+ years of sterility testing expertise, the Steritest® System has continuously evolved to deliver smarter, safer, and more reliable closed-system testing workflows — fully compliant with USP <71>, Ph. Eur. 2.6.1, and JP <4.06>.

Our broad portfolio allows you to configure your Steritest® system to fit your sample type, packaging format, and controlled testing environment — whether in a laminar flow hood or isolator. All Steritest® NEO devices are equipped with the Velax® cutting clamp, eliminating scissors from the workflow and reducing contamination risk, and feature a 2D Data Matrix barcode (Q4 2026) on each canister for seamless integration with LIMS and ERP systems. A range of ergonomic accessories, including sampling solutions for further subculture or identification purposes, further optimizes convenience and safety at every stage of the test.

Designed to work seamlessly with M-Trace® software for full digital traceability, our portfolio includes:

Operator scanning a rinsing fluid bottle during a Sterility Test to capture the data into the M-Trace software

Today's laboratories are shifting toward fully digital, guided workflows where every action is recorded contemporaneously, creating a complete, end-to-end test lifecycle. Regulators require data to be attributable, legible, contemporaneous, original, and accurate (ALCOA++), and FDA 21 CFR Part 11 mandates that electronic records and electronic signatures meet strict integrity and audit trail standards.

Our digital QC solutions, the M-Trace® software & Mobile App are engineered to meet exactly these expectations: linking data from pumps, consumables, and samples into a single, auditable Master Test Record that supports faster investigations, more robust regulatory filings and ensuring full compliance with 21 CFR Part 11 and data integrity requirements (ALCOA++).

While step-by-step guidance and real-time deviation alerts increase process safety.

  • Guided QC workflows with voice or on-screen instructions
  • Real-time deviation alerts for immediate corrective action
  • Paperless recording and review — from pump to audit trail
  • Desktop & mobile app access for flexible operation
Operator reading the results of a rapid sterility test with the Milliflex Rapid system

Based on highly sensitive ATP bioluminescence technology — now recognized under USP <73> (ATP Bioluminescence-Based Microbiological Methods for the Detection of Contamination in Short-Life Products) effective August 2025 — The Milliflex® Rapid System 2.0 enables faster release decisions for short shelf-life products such as cell and gene therapies, without compromising regulatory compliance.

The Milliflex® Rapid System 2.0 is an automated solution for the rapid detection, imaging, and quantification of viable microbial contaminants in filterable samples.

  • Results in 5 days or less — compared to the traditional 14-day test
  • Versatile for diverse organism types, including slow growers
  • 21 CFR Part 11 compliant, with full audit trail support
  • Easy handling & straightforward validation package
  • Suitable for both sterility testing and bioburden monitoring

Expert support for your sterility testing — from implementation to routine operation, and beyond

Operator performing a performance qualification of the Steritest Symbio pump for Sterility Tests

Our commitment doesn't stop at the product. From implementation to routine operation, our team of experts is here to support you at every stage of your sterility testing program.

Equipment Services:

  • Installation, Qualification, and Performance Qualification (IQ/OQ/PQ) for Steritest® Symbio pumps and Milliflex® Rapid System
  • Preventive maintenance and calibration services
  • Consulting for system setup, workflow optimization, and regulatory readiness

Training:

  • Hands-on operator training on Steritest® NEO devices, Symbio pumps, and M-Trace® software
  • Application training for the Milliflex® Rapid System at our dedicated applications lab
  • Regulatory-aligned training supporting USP, Ph. Eur., and 21 CFR Part 11 compliance requirements

As USP highlights, sterility testing should only be performed by personnel trained to independently conduct a microbial test — our training programs are designed to meet exactly this standard.


Related Resources

Page 1 of 4