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Gary Smith

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Gary Smith, PhD

Gary Smith, PhD

Born and raised in Caddo County, Oklahoma, Dr. Gary Smith attended universities in California, Washington and Texas. Since 1961, he has taught and conducted research at Washington State University (WSU), Texas A&M University, and Colorado State University (CSU).

From 1961 to 1975, his research focused on beef palatability (bullocks vs. steers, carcass chilling effects on tenderness, blade tenderization, electrical stimulation of carcasses, Tenderstretch®); beef shelf life (vacuum packaging for domestic and transoceanic shipments, retail case life); and USDA Feeder Cattle Grade Standards From 1975 to 1990, his research efforts included modified atmosphere packaging of beef; transoceanic shipments of variety meats; USDA Beef Quality and Yield Grade Standards; time-on-feed and beef palatability; The Hamburger Steer®; breed types and beef palatability; beef lipids and human nutrition; National Consumer Retail beef Study; and restructured beef steaks.

From 1990 to 2015, his research focused on chemical residues in US beef; National Beef Quality Audits; International Beef Quality Audit; National Market Cow and Bull Audits; injection site lesions; Conventional, Natural, and Organic Beef; feeding Vitamin E and Beef retail case life; “Multiple-Hurdle E. coli 0157:H7 decontamination systems; implementation of HACCP programs in beef packing plants; Palatability Assurance Critical Control points; controlling Salmonella and Listeria on ready-to-eat beef; Best Practices for mitigating BSE (Mad Cow Disease) risk in packing plants; traceability systems implementation; and instrument grading of beef carcasses. Dr. Smith credits his success to colleagues and graduate students (who did the hard work) and the help of cattle feeders, packers, and retailers (who allowed them to use their facilities and products).

Dr. Smith occupied the Ken and Myra Monfort Endowed Shair in Meat Science at CSU beginning in June of 1990. Previously, he served as Professor (1969-1982) and Head (1982-1990) of the Department of Animal Science at Texas A&M where he received many awards.

  • Outstanding Teaching Performance Award,
  • Honor Professor Award
  • College of Agriculture Teaching Award
  • University Distinguished Teaching award
  • Deputy Chancellor’s Award for Team Research

Other awards and honors include:

  • International Stockmen’s Hall of Fame Induction
  • National Cattlemen’s Foundation Vision Award
  • USMEF Distinguished Service Award
  • AMSA R.C Pollock Award
  • Beefmaster Breeders United, Commitment to Excellence Award
  • Honored Researcher of the CSU Research Foundation
  • ISI Thomson Scientific’s Highly Cited Researcher
  • Beef Magazine’s top 40 Most Influential People in the US Beef Industry
  • American Hereford Association Hall of Merit Induction
  • Meat Industry Hall of Fame Induction
  • AMSA Mentor Award
  • Cattle Feeder’s Hall of Fame Award
  • College of the Sequoias, California State University-Fresno and WSU Distinguished Alumni Award
  • Certified Angus Beef Industry Achievement Award

Below are resources from Dr. Smith:



Ensure compliance and product safety with Eurofins' USP Microbiology Services. Learn how USP Testing and Suitability Testing help validate methods for dietary supplements, probiotics, and botanicals while avoiding false negatives and regulatory pitfalls.


Low water activity foods (LWAFs) have historically been considered low-risk for microbiological hazards because their limited “free” (unbound) water in the formulation prevents bacterial growth. However, foodborne illness outbreaks revealed that pathogens can survive for extended periods in LWAFs, even in the absence of growth. Watch now to learn what is required to validate control measures to reduce microbial risks in LWAFs. Originally Aired on June 18, 2025.


Whether you're formulating a botanical powder, validating a nutrient claim, or verifying supplier specifications, reporting on a dry matter basis ensures that decisions are grounded in reliable, standardized data. Click to read a simple explanation of dry matter basis reporting, when it matters, and why.


Fortifying foods and dietary supplements with vitamins, minerals, and bioactives has become a key strategy for innovation and value. Understanding and planning around the LOQ is vital to protecting both your product integrity and your brand credibility. Continue reading to learn how to proactively evaluate your nutrient levels against assay capabilities.


You believe in your ingredient. You’ve seen the research, tested the science, and refined the story. But for buyers, belief isn’t enough—it needs to be experienced. That’s where a pilot plant makes all the difference. Read our blog to learn about the value of a pilot plant for ingredient suppliers.


Join us as we explore key test methods designed to evaluate a protein ingredient’s application potential—its functionality fingerprint. This webinar showcases how these tests can drive product innovation and includes real-world examples and case studies to demonstrate how this approach has brought insights to life. Originally Aired on May 29, 2025


High-value edible oils like olive oil and avocado oil command premium prices for their flavor and health benefits. However, their value also makes them targets for degradation and food fraud. Read our blog about two complimentary testing approaches essential to protecting your customers and brand: quality testing and authenticity testing.


Explore the food safety concerns surrounding Bisphenol A (BPA) in packaging, its potential health risks, and emerging alternatives like BPAF, BP, BPF, and BPS.


Effective risk assessment is essential for ensuring dietary supplement safety, regulatory compliance, and brand integrity. Learn how to protect quality and consumer trust.


Explore the critical role of vitamin K in health and the importance of accurate testing for infant formula, food, beverage, and supplement industries. Learn about the latest techniques and troubleshooting strategies to ensure reliable measurement.


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