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John Scanga

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John Scanga, PhD

John Scanga, PhD

Chief Scientific Officer for North American Meat Division

John received his B.S. degree in Animal Sciences, his M.S. degree in Meat Science in 1997, and his Ph.D. in Animal Sciences in 1999, all from Colorado State University in Fort Collins, CO.

He developed a connection to agriculture at an early age; through work on his family’s ranching operation in central Colorado. He enrolled at Colorado State University in the fall of 1992 majoring in Animal Sciences; he competed on the CSU Meat Judging Team in 1994 and worked as an employee in the meat laboratory where his interest in meat processing and the meat industry began to grow.

Following the completion of his M.S (1997) and Ph.D. (1999), John joined the faculty at Colorado State University as an Assistant Professor and Extension Meat Specialist. He managed the day-to-day operations of the Meat Science Teaching and Research Laboratory and was promoted to Associate Professor in 2005.  He then left the university and joined IEH Laboratories and Consulting Group in January of 2008 as Vice President of Technical Services, where he continued to merge scientific concepts with industrial applications for managing and improving the safety of meat and non-meat foods, and improving food processing plant operational efficiencies.  In addition, he provided clients with regulatory, crisis event, and HACCP training and support.

John joined Elanco Animal Health in November of 2009 as an Associate Senior Technical Consultant where he brought a consumer focus and an emphasis on balancing animal productivity and performance with consumer acceptability. His work there focused on red meat safety, red meat quality and international trade.

John has been an author or co-author on over 70 refereed scientific publications on red meat quality and safety and has presented the findings of his work through numerous invited in presentations both the U.S and internationally.  

John also has a passion for service.  He currently is the chair of the Colorado Beef Council and has served as President of the Weld RE-9 school board, Weld County Fair Board and is a member of the Highland High School FFA Advisory Committee. 

John and his wife Chauna live on a diversified farming operation in Ault, Colorado.  Their family time is consumed with agriculture, farming, riding reigning horses and traveling.  His hobbies include backcountry snowmobiling and bird hunting. He  also works as a visiting professor in the Department of Animal Sciences at Colorado State University, where he first started his academic career. 

Below are resources from Dr. Scanga:



With innovation comes complexity and with complexity comes risk. This is why laboratory testing isn’t just a box to check. For longevity products, it’s one of the most challenging and essential parts of responsible product development.


California’s SB 646 represents a major advancement in prenatal supplement safety. By mandating rigorous testing and transparent reporting of heavy metal levels, the state is setting a new benchmark for protecting pregnant individuals and their developing babies.


In today’s food and dietary supplement marketplace, trust is no longer assumed. Third-party testing and certification have become essential tools for demonstrating product safety, quality, and compliance in a credible way.


There has been a lot of talk about the Dietary Guidelines for Americans (DGA) that have been recently published. Despite being promoted as a major departure, the updated guidelines mix a few foundational changes with many recurring themes from earlier publications.


For manufacturers and brand owners, dietary fiber is more than a buzzword, it’s a key driver of product positioning, consumer trust, and regulatory compliance. But not every ingredient marketed as “fiber” qualifies under FDA standards. Keep reading to learn more about why understanding fiber is so important.


Choosing safe, high-quality food and dietary supplement products has become increasingly complex. Product labels are filled with claims, ingredient lists can be difficult to interpret, and rumors about lack of regulatory oversight run rampant across social media and elsewhere. Third-party product certification is the answer.


In today’s supplement marketplace, contract manufacturers play a pivotal role. As retailer expectations evolve and third‑party verification becomes increasingly important, product certification is no longer just a valued add, it’s becoming a strategic advantage. Click to learn more about the benefits of product certifications.


As we look back on 2025, one thing is clear: innovation didn’t slow down, it got sharper. Across major food, beverage, supplement, and ingredient tradeshows this year, the conversation shifted away from flashy novelty and toward proof, performance, and practicality. Here is our perspective on what to expect in 2026.


How do you know when it makes sense to bring in product development support and when it doesn’t? Based on what we see across brands, ingredient companies, and startups, here’s a practical way to think about it.


Ethylene glycol (EG) and diethylene glycol (DEG) are toxic industrial chemicals that have no place in consumer health products. Unfortunately, products ranging from cough syrups to dietary supplements have been found to contain these contaminants, often with tragic consequences.


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