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Why do pathogen tests take days when the detection methods (like PCR) can be completed in just a few hours? Dan DeMarco, Ph.D. from our Eurofins Microbiology lab in Louisville, KY discusses this topic in this short video. Eurofins publishes our Ask an Expert Series weekly on our social media platforms.


Taking Control of Food Spoilage and Safety in the Era of Food Microbiomics


In this webinar, Jeff Stassi and Lukas Vaclavik will discuss testing for both contaminants and adulterants in your products. Also, the importance of designing the proper monitoring program to ensure your products are safe and compliant. Original airdate June 20, 2023.


In this webinar, Eurofins and AFIA come together to provide updated information on the Safe Feed/Safe Food Version 7.0 changes.


Botanical reference materials play a critical role in herbal product testing. Learn about the importance of botanical reference materials, and how choosing a lab with a large reference material library impacts analytical outputs.


Are you incorporating novel or upcycled protein materials in your products? This handout describes a key issue surrounding traditional determination, calculation, and labeling of two compulsory nutrients (protein & carbohydrates) in the US Nutrition Facts Panel.


Our webinar hosted by Dr. Neal Craft, Chief Scientific Officer of Eurofins, explores the world of natural pigments, testing methods, and unique matrix challenges.


At Eurofins, ExpressMicro samples arrive at the lab in the early morning hours, six to eleven hours earlier than other labs—and we deliver results up to eight hours faster than standard next-day air shipping.


Eurofins Microbiology Laboratories, Inc (Lafayette, CO) is excited to announce it has been certified by the Colorado Department of Public Health and Environment (CDPHE) to conduct microbial hemp compliance testing for industrial hemp and hemp derived products.


Eurofins accepted a request to perform testing compliant with 21 CFR Parts 210/211 on an excipient material for over-the-counter pharmaceutical products and develop specific test methods to support the risk assessment of the manufacturing process and batch release. Read about what happened in response to the OOS test results.


 

 

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