Gary Smith

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 1916 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:

Reformulating Without Artificial Dyes: Why Stability Studies Are Critical

As consumer demand for cleaner labels and naturally derived ingredients continues to rise, many manufacturers of OTC and dietary supplement products are reformulating to remove artificial colors and dyes. While this shift aligns with market trends, it introduces significant challenges—especially when it comes to product stability.

Keywords: Blog Contaminants Shelf Life Supplements OTC

Eurofins' Ian Laessig on OTC GMP Testing Processes

In this video, Business Unit Manager Ian Laessig shares how the Eurofins team collaborates with OTC and GMP clients to ensure compliant testing and a seamless experience.

Keywords: Video OTC

Eurofins' Ian Laessig on Supporting the OTC and GMP Industries with Testing

In this video, Business Unit Manager Ian Laessig explores how Eurofins Food Chemistry Testing supports the OTC and GMP industries with comprehensive testing solutions for APIs in finished products, ingredients, and excipients.

Keywords: Video OTC

From Principle to Practice: Specialized Testing for Homeopathic Products

Homeopathic formulations can be complex and challenging to test. A client approached Eurofins Supplement & OTC Testing in Madison, WI needing specialized testing of homeopathic tinctures. Read our case study to learn how the client was able to confidently release their product while maintaining compliance and efficiency.

Keywords: Case Study Special Investigations OTC

Ensuring Drug Quality: An Overview of 21 CFR Parts 210 & 211

The Food and Drug Administration (FDA) monitors drug manufacturers' compliance with its current Good Manufacturing Practice (cGMP) regulations in order to ensure the quality of drug products. These regulations are designed to assure products are safe for use and contain the ingredients, strengths, and efficacies of claims made by the product. Learn what tests your OTC products need to be compliant.

Keywords: Blog OTC Shelf Life & Stability ID & Purity Authenticity

APIs in Gummy Matrices: Revolutionizing Drug Delivery

The world of wellness is experiencing a “gummification” wave, which includes using gummies to deliver APIs as a replacement for traditional forms like pills and syrups. But this matrix doesn't come without challenges. Click to read how you can ensure the effectiveness of alternative forms like gummies, chews, drink mixes, and lozenges.

Keywords: Blog OTC Supplements

On-Demand Webinar - Navigating the Intersection of Technology, Standards Development, and Regulatory Compliance in a Changing Administration

This webinar explores approaches to method and monograph development while maintaining safety and quality standards specific to the OTC and Dietary Supplement industries. The speakers share industry insights regarding current state and potential changes with a changing administration. Original Air Date: February 24, 2025.

Keywords: Webinar Supplements OTC Regulatory

Developing Custom Test Methods to Generate Data for the Risk Assessment of the OTC Manufacturing Process and Set Batch Release Criteria

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.

Keywords: Case Study Special Investigations OTC

Case Study: Pharmaceutical tablet discoloration

Foreign materials in products can be dangerous to consumers and damage a brand's reputation. At Eurofins, we have the expertise and experience to handle all kinds of foreign material investigations, including issues in pharmaceuticals and dietary supplements. This case study outlines how we used microscopy and elemental analysis to determine the cause of discoloration in a pharmaceutical tablet.

Keywords: Case Study Special Investigations Supplements OTC

Food Dye Testing White Paper

Natural and synthetic food dyes are used in almost all industries. Understanding the potential for dye adulteration is critical to knowing how and why products are affected. Furthermore, testing with a third-party lab can lead to standardized product coloration and reliable ingredient claims. This White Paper introduces the types of food dyes, the benefits of testing, types of tests, and considerations for choosing a third-party lab.

Keywords: Scientific Research Authenticity Food Beverages Supplements Ingredients OTC

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