Resource Library
Welcome to the Eurofins US Food, Feed, and Supplement testing laboratories resource library.
Here you will find blogs, webinars, scientific articles, videos, case studies, white papers, and more about the services we offer for your industry. If you are looking for something in particular please use the search bar to search our whole library.
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As part of an effort to promote public health, the FDA has proposed a rule to change the definition of “healthy” on food labels. Our infographic gives background on the proposed rule and a high-level view of the proposed criteria. Originally Published on December 18, 2024.
Your goal is to manufacture a safe product that meets the claims on your label.
How are you ensuring that your finished product will do this?
Proactively, or retroactively?
Putting a proactive plan in place to assess ingredient safety and quality is key to producing finished products that meet all of your quality standards. Having a partnership with an accredited, independent (third-party) laboratory just in case something goes wrong is a must.
Validation of aseptic fillers intended for the production of low-acid, shelf-stable products is a core requirement of the FDA’s low-acid canned food (LACF) regulations (21CFR113 and 108.35). Microbiological challenges of the aseptic zone and packaging material sterilization cycles are important components of the validation process. These challenges are often conducted at the production site using non-pathogenic surrogate organisms that mimic the resistance of the pertinent target pathogen. This presentation will provide a brief history of the use of such surrogates for the validation of low-acid aseptic fillers along with the approach we have used to qualify the surrogates as adequate for the intended technology.”
As a manufacturer of specialty pet food or pet food products, how will Pet Food Label Modernization (PFLM) affect your business? In this blog, we help you decipher high-level changes coming with PFLM, including how to prepare for the updated guidelines.
This article describes the basics of flow cytometry in its application to probiotic enumeration, including a comparison between flow cytometry and traditional plate count methods, afu vs cfu, advantages and disadvantages of flow cytometry, marketplace examples and investigative case studies.
Mushroom toxicity comes from many sources, including the soil, processing, and the mushrooms themselves. This infographic outlines sources of contamination, as well as steps to take to minimize the risk of toxins entering the food chain.
IR spectroscopy, including NIR and mid-IR, is a useful technology for food and beverage analysis. The experts at Eurofins QTA recently answered five common questions about IR spectroscopy to help you determine if it is right for you and your products. This infographic provides an overview of how IR spectroscopy is helpful for product analysis.
December 1st, 2023
Eurofins is excited to announce Nick Johnson has joined the team as the Regional Sales Manager at Eurofins Microbiology Laboratories in Tustin, California.
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November 2023
Eurofins is pleased to announce the appointment of Justin Eason as the new Business Unit Manager for our North Carolina laboratory.
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Eurofins presents a validation of USP <467> residual solvent methodology for testing on CBD and hemp-based products at the North American Chemical Residue Workshop.