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Today’s pharmaceutical landscape is more vibrant than ever. While new modalities such as mRNA and an ever-increasing number of biosimilars help make critical vaccines and therapies available to more patients in need, they also put pressure on manufacturers to control costs to deliver these drugs while remaining profitable. 

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

Creating value through efficient quality monitoring

With hundreds of steps required to manufacture a biologic, monitoring your product and process at key points gives you the confidence that your batch quality is secure.

Rapid and automated technologies for both in-process and release testing increase the efficiency of your operations through standardization - reducing the cost of non-quality by cutting costs from scrap, investigations, downtime, decontamination, and additional human resources.

Our user-friendly platforms will not only help make your lab workflow more efficient and improve your team’s work environment but also reduces risk of error and increases data integrity and traceability. Collectively, these improvements increase efficiency of each technician which can reduce reliance on costly outsourcing of testing.

Product List


    Em-body Connectivity

    Monitoring quality in microbiology is critical and challenging for pharmaceutical companies. ​While hand transcription remains the standard procedure in use, these daily processes often rhyme with errors leading to time-consuming investigations, and not fully compliant data.​

    Em-power the Future

    Environmental monitoring (EM) is the main microbiological control performed by pharmaceutical industries. While multiple hand-written and transcription operations remain the standard procedure in use for thousands of samples per month, the daily processes often result in errors leading to time-consuming investigations, low value-added tasks and data that is not fully compliant. As a result: major impacts on batch release, on process efficiency and ultimately patient safety.

    Em-brace Traceability

    The 3P® legacy is one of delivering proven performance when it comes to effective pharmaceutical contamination control. Now it’s going digital.
  • AIR IDEAL® 3P®

    Bring Confidence to your Environmental Monitoring

    AIR IDEAL® 3P® is used for the detection of viable organisms through active air sampling.
  • API® 

    Manual Microbial Identification

    API® makes microbial identification simple and reliable. Combining a standardized method with an extensive and robust digital microbial ID knowledge base, API® can easily be implemented into any microbiology laboratory.

    Patented Colormetric Technology

    The BACT/ALERT® 3D was developed as an effective and safe solution for industrial sterility testing.
  • BIOBALL® Standardized Strains

    Microbiological Quality Control

    BIOBALL® is a small water-soluble ball containing a precise number of microorganisms that delivers accuracy and precision, batch after batch.
  • BIOBALL® Custom Services

    BIOBALL® Custom Services helps you simplify the implementation of microbial strains of your interest in the routine microbiological quality control.
  • BIOFIRE® Mycoplasma

    Rapid Testing by Anyone, Anywhere, Anytime

    BIOFIRE® Mycoplasma provides simple, accurate, and rapid in-house mycoplasma detection for use in testing raw materials, in-process samples, and final product release. We offer validation services designed to meet regulatory requirements—from documentation to comprehensive on-site support.

    Better for your lab. Better for the planet.

    ENDONEXT™ endotoxin detection assays are ushering in a new era of smarter, more sustainable pharmaceutical quality control.