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In this blog post Eurofins Analytical Services Manager Jeff Stassi explains why it is so important to set specifications for dietary supplements.


In this blog post Jeff Stassi, Eurofins Analytical Services Manager, gives three tips on how to make sure that you are partnering with a testing laboratory that you can trust, and that has the expertise required to analyze your product.
Keywords: Blog Supplements


Learn more about the similarities and differences between the terms: fraud, defense, authenticity, and adulteration when it comes to foods, ingredients, and supplements.


This white paper will provide a brief overview of both prevention and investigation of spoilage. By focusing on principles, it will not be able to answer every question, but rather will illustrate questions to ask during product design and failure investigations.


The southwest leafy green industry has once again completed its migration south and Eurofins Microbiology Laboratories Yuma is ready. This year the lab has upgraded to better support the industry.
Keywords: News Produce


Both Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) can apply to testing needed for your raw materials and products. Learn how they apply during different phases of the product development process.


What really is dietary fiber according to the most recent FDA regulations? This blog will help break down the FDA’s most recent definition of fiber as well as provide examples of ingredients used in the industry today.


Here we highlight the best practices in process validation that pet food manufacturers may use to scientifically demonstrate that a given process, or “kill step,” in the manufacture of pet food and pet food products can deliver the required microbial reductions to ensure the safety of their product. 


As a food manufacturer, you have several options for adding sweetness to your product, including sugars, sugar alcohols, and artificial sweeteners. But how do they compare, and how do they impact the caloric content of your final product?
Keywords: Blog Nutritional


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.


 

 

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