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Create Value by Harvesting the Full Potential of your Bioprocessing Testing

Bioprocessing Solutions

In the dynamic world of biopharmaceutical manufacturing, ensuring the highest quality and strict compliance is essential. Explore how our cutting-edge microbiological quality control solutions can enhance your operations and optimize quality assurance.

Enhance Workflow Through Efficient Quality Monitoring

While there is no single solution to increasing operational efficiencies and reducing costs of non-quality, industry experts agree that automating routine analytical testing brings value by reducing costly errors; providing reliable, actionable and traceable data faster; and increasing throughput to reduce bottlenecks.

We are proud to be Your Ally in Advancing Quality by providing the most comprehensive portfolio of microbiology quality control solutions to monitor your products, process and environment.

Our solutions not only enhance your laboratory workflow but also foster a better work environment for your team. By increasing technician efficiency, you can reduce reliance on costly outsourcing for testing, ultimately contributing to a more sustainable and profitable operation.

Elevate your biopharmaceutical manufacturing process with our innovative testing solutions, helping ensure the highest standards of safety and quality in every batch.

   

    

Are You Securing Quality Throughout Your Biopharmaceutical Production?

With hundreds of steps in biologic manufacturing, it's essential to monitor your product and processes at critical junctures. Our rapid and automated technologies for both in-process and release testing enhance operational efficiency through standardization. This approach reduces the cost of non-quality by minimizing waste, investigations, downtime, and the need for extensive human resources.

    

Discover Our Proven Portfolio of Value-Added Bioprocessing Solutions

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Bioprocessing Solutions

  • 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® 2 COMPACT

    Your Solution for Automated Microbial Identification

    The VITEK® 2 Compact system offers quality control testing solutions for fast and accurate microbial identification. With technology that includes an extensive and robust identification database, rapid results, and minimal training time, it will streamline laboratory workflow for increased productivity.
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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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Contact Our Experts For More Information On Our Bioprocessing Solutions

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Learn More About Our Bioprocessing Solutions

Streamlining Pharmaceutical Quality: The Power Of Automated Environmental Monitoring

Traditional, manual methods of environmental monitoring can be subject to numeration errors as well as data traceability and integrity issues, which result in overall inefficiency. Want to uncover how automated methods outperform these traditional approaches? Download our infographic now and gain exclusive insights.
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Automated 1 Hour Mycoplasma Detection in Bioproduction

Various pharmacopoeias, including the USP, specify a test for mycoplasma contamination must be performed as part of the release testing of a product manufactured in the presence of eukaryotic cells (1).
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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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