The new cleanroom at our global headquarters in Salt Lake City, Utah, was designed for today's rigorous contamination control expectations, driven by EU GMP Annex 1. Learn More
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On-Demand Webinars



Learn from our experts on industry topics.



Webinar: Testing of High-Risk Drug Components for Diethylene Glycol and Ethylene Glycol

Contamination from ethylene glycol and diethylene glycol in liquid formulation poses a high risk to patient safety. Throughout recent years...

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Biocompatibility Testing: What You Need to Know

When it comes to biocompatibility testing on medical devices, there are many aspects that have to be considered not only...

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Advancing Microbial-Contamination Detection Through Rapid Sterility Testing

Increasing industry and product demand for expedited product release reinforces the need to embrace rapid sterility technologies. Nelson Labs is...

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What’s New with Reprocessing Validations for Reusable Medical Devices?

There have been many great strides surrounding the guidance for reprocessing (cleaning, disinfection, and/or sterilization) validations for reusable medical devices....

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Disinfectant Efficacy Testing on Site Specific Surfaces

Disinfection efficacy studies play a significant role in the Pharmaceutical manufacturing environment in ensuring that the surfaces are adequately sanitized...

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