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503A Compounding, 503B Outsourcing, and Hospital Pharmacies

Microbiological quality control is a critical step in developing and releasing compounded or customized medications. Every step in the process helps ensure treatments are safe for patients. While essential, it can be labor-intensive and time-consuming, sometimes requiring days to receive results.

That’s where our solutions come in. From sterility results in as little as four hours to MALDI-TOF identification and smarter, more sustainable endotoxin testing, we offer a comprehensive portfolio of rapid microbiology solutions designed to improve efficiency—enabling faster batch releases and a more reliable supply.

Microbiological Quality Control Solutions for Compounding Pharmacies and Hospital Pharmacy Operations

With demand for customized medications continuing to grow, compounding pharmacies have a unique opportunity to capitalize. A streamlined, automated quality control workflow that delivers fast, accurate results can be a key differentiator.

Whether you’re looking for increased speed, enhanced sterility assurance, greater regulatory confidence, scalability—or all of the above—bioMérieux has you covered.

Our Microbiological Quality Control Solutions

  • Pharmaceutical Culture Media

    Comprehensive Control

    Reliable culture media solutions safeguard pharmaceutical products from contamination, making them an integral part of microbiology QC testing. Production of our culture media follows rigorous quality control procedures, from formula development to validated performance.

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  • VILINK® Instrument Management System

    Instrument Management System

    VILINK® software is our real-time support system that keeps the instruments in your laboratory running via remote monitoring.

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  • VITEK EXPRESS Identification Services

    ID Services Powered by Microbiology Experts

    As microbiologists, we know fast and reliable results are of the utmost importance. Get the accurate identifications you need quickly and easily.

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  • VITEK® MS Rapid Identification of Microorganisms

    Improve Your Productivity and Increase Confidence

    VITEK® MS was developed for its rapid identification of microorganisms for the pharmaceutical,personal care, and food industries. Suitable for industrial manufacturers and pharmaceutical laboratories who work with microbial identification, our knowledge base contains the most frequently encountered organisms in pharmaceutical, food and animal health applications.

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  • VITEK® MS PRIME MALDI-TOF Mass Spectrometry System

    Superior Workflow. Prime Results.

    The VITEK® MS PRIME is an innovative MALDI-TOF mass spectrometry system that takes your automated identification experience to the next level.

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Partner With bioMérieux To Increase QC Efficiency 

Want to enable compliance confidence and faster batch releases?

Complete the form below to get in touch with our team. A bioMérieux expert will be in touch using the contact information you provide. By providing your information, you agree to receive additional emails from bioMérieux about microbiological quality control testing. 

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Validation and Successful Implementation of SCANRDI

CASE STUDY

Validation and Successful Implementation of SCANRDI®

This case study outlines the process Atlas Analytical used to demonstrate that the SCANRDI® technology is qualified for determining the sterility of test samples.

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ARTICLE

Single vs. Dual Temperature Incubation in Environmental Monitoring

Single temperature incubation is less commonly used in environmental monitoring today — but that’s starting to change. This article explores how the right strategy and tools can help your program shift to a single temperature approach for greater efficiency, simplicity, and risk reduction.

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EBOOK

Your Quick Guide To Better Endotoxin Testing

Most new users of Limulus-based tests want to review basic knowledge around endotoxin and endotoxin detection, while more experienced users want to review the practical aspects of testing with an eye toward meeting ever-changing regulatory expectations. They also want to generate laboratory dialog as to how to apply basic principles and “best practices” to increasingly complex tasks including method development, verification, validation and the routine testing of various drug types. This material can also serve as a supplement to a user’s basic endotoxin training.
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