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Douglas L. Marshall

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Douglas L. Marshall, PhD, CFS

Douglas L. Marshall, PhD, CFS

Chief Scientific Officer

Dr. Marshall is Chief Scientific Officer with Eurofins Microbiology Laboratories, Inc., a division of the global life sciences company Eurofins Scientific.  He is co-founder and Director of the Food Safety Institute, LLC, an integrated consulting and analytical services company affiliated with the Eurofins network of companies.  He is Technical Director for the Refrigerated Foods Association and Microbiology Task Force Chair for the American Spice Trade Association.  His former positions include the following:

  • Associate Dean and Professor of Public Health, College of Natural and Health Sciences, University of Northern Colorado
  • Adjunct Professor with the Colorado School of Public Health and Colorado State University
  • Professor of Food Science, Nutrition, and Health Promotion at Mississippi State University
  • Assistant Professor of Food Science at Louisiana State University
  • Contributing Editor for the peer-reviewed scientific journal Food Microbiology
  • Four consecutive terms on the editorial board of the Journal of Food Protection

He is a frequent volunteer and consultant to trade associations, NIH, WHO, FAO, USDA, and other government agencies and private companies.  His research and expertise has been featured in popular press venues such as Consumer’s Reports, Fine Cooking, USA Today, Fitness, Health, Men’s Health, Chemtech, Nature Science Updates, and ASM Journal Highlights.  He is a frequently invited speaker and a prolific book chapter writer. With over 250 publications, over 300 invited presentations, and over 100 workshops delivered, his scientific research and outreach interests focus on improving the microbiological quality and safety of foods, with emphasis on meat, poultry, seafoods, and produce.  Among these was the completion of the 4 volume Handbook of Food Science, Technology, and Engineering, which he Co-Edited.  He has been the recipient of a number of awards for his scholarly efforts including the Mississippi Chemical Corporation Award of Excellence for Outstanding Work, the International Association for Food Protection Educator and Harold Barnum Industry Awards.  He is a Fellow and former member of the Board of Directors of the Institute of Food Technologists, inaugural Chair of the International Food Science Certification Commission, and former member of the Board of Directors of the American Spice Trade Association. 

On a personal note, early in his career he served as a deck hand on an Alaskan fishing vessel (well before Deadliest Catch) and prefers to spend his free time lost on a trail in the Colorado Rocky Mountains.

Below are resources from Douglas:



Food fraud, also known as economically motivated adulteration, is widespread worldwide.  Food fraud involves deliberate and intentional substitution, addition, tampering or misrepresentation of food, food ingredients or food packaging, labeling, product information or false or misleading statements made about a product for economic gain.  Food fraud can adversely impact consumer health, product quality, and brand reputation.


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


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.


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.”


New options for sweetening low-sugar foods have entered the market. Testing of sweetener ingredients and the finished product is key.


While many vitamins are traditionally sourced from animal products, plant-based vitamin sources are a growing trend. Learn more about this new trend and what this means in regard to testing your products.


Method validation, method verification and fitness for purpose all seem similar, but each requires a distinct level of evaluation and different considerations. Learn more about their similarities and differences in this article.


Candies can now give you more than a sugar rush. Functional chocolates also have vitamins, minerals, and botanicals and with that means the need for suitable validated methods to verify claims. Eurofins is your partner is all challenging vitamin, mineral, and botanical testing in finished products and raw materials.


Is Front-of-Package Labeling right for you? Learn how Front-of-Package Labeling affects nutritional value and market sales, and how Eurofins can help with testing your products and generating nutritional and dietary supplement facts panels.


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