Panel discussion on...
Pet Supplements
Maggie McNamara
VP of Global Marketing, Saanroo

Member of AgroFOOD Industry Hi Tech's Scientific Advisory Board

Pet Supplements: Quo Vadis?
From Treats to Trust: The New Era of Pet Wellness
1B) Species-specific research is critical to pet supplement development, even when an ingredient has a strong foundation of human clinical data. While human research can provide valuable insight into biological mechanisms, particularly for endogenous compounds such as palmitoylethanolamide (PEA), it cannot fully account for differences in metabolism, receptor expression, digestive physiology, and behavioral indicators of health across species (1, 2, 3).
Human data may inform hypothesis generation and safety considerations, but responsible pet formulation ultimately requires evidence that reflects animal-specific biology. This includes careful consideration of dose, absorption, and appropriate outcome measures that align with how comfort, mobility, or overall well-being are expressed in companion animals (1, 2, 3) Without this context, there is a risk of over-extrapolation that can undermine scientific credibility (2, 3).
1D) Quality parameters such as standardization, purity, and bioavailability are especially critical in pet supplements (4, 5, 6). Animals cannot self-report outcomes, so consistency and predictability of ingredient performance are essential (3, 4).
For lipophilic compounds such as PEA, bioavailability is a key consideration. Without appropriate formulation strategies, absorption can be inconsistent, leading to variable outcomes (4, 5). Standardization ensures reproducible active content across batches, while purity minimizes the risk of unintended effects in sensitive populations (3, 4, 5, 6). Together, these parameters support both scientific rigor and responsible product development (3, 4, 5, 6).
1F) While randomized, placebo-controlled clinical trials remain the gold standard, they are not always practical at scale in companion animals. A layered evidence approach is often more realistic and scientifically responsible (7, 8, 9).
For ingredients such as PEA, this may include peer-reviewed human clinical research establishing safety and biological mechanisms, supported by translational or preclinical studies and well-designed observational research in pet populations (1, 7, 8, 9). Transparency around study design, endpoints, and limitations is essential. Claims should reflect the strength and scope of the available evidence rather than extending beyond what data can reasonably support (8–9).
1G) Claims related to inflammation, comfort, pain, or aging are among the most frequently misunderstood in the pet supplement space. When biological pathways are discussed without sufficient context, consumers may interpret supportive claims as therapeutic promises.
This risk can be reduced through precise language that emphasizes physiological support rather than treatment outcomes. For ingredients like PEA, focusing on mechanisms of action and biological pathways, rather than implied results, helps align consumer expectations with scientific reality (1, 2, 10). Clear substantiation and transparent communication are key to maintaining trust (3, 10, 11, 12).
1L) Yes, there is a growing focus on healthy ageing in pet nutrition, reflecting broader trends seen in human health. As companion animals live longer, interest has shifted toward supporting comfort, resilience, and overall quality of life rather than addressing isolated symptoms (1, 13, 14).
Ingredients such as PEA are increasingly examined within this context due to their involvement in inflammatory balance and cellular signaling pathways (1, 2, 13). The challenge for the industry is to translate these insights responsibly, ensuring that ageing-related positioning is grounded in evidence and communicated without overstating outcomes.
4A) The long-term credibility of the pet supplements sector will depend on its commitment to scientific discipline, transparency, and evidence-aligned communication. Greater emphasis on species-relevant research, realistic claims, and standardized substantiation practices will be essential.
In this Panel Discussion, several prominent companies within the food and nutraceutical ingredient industry have been invited to discuss about drivers and barriers of healthy lifestyle, focusing on global and regional consumer trends, scientific achievements, emerging delivery formats, use of AI technologies and the implementation of the United Nations sustainability goals.
Panelists
References and notes
- Abramo F, Campora L, Albanese F, et al. Palmitoylethanolamide and related ALIAmides for small animal health: evidence from preclinical and clinical studies. Animals. 2022;12(17):2226. https://pmc.ncbi.nlm.nih.gov/articles/PMC9496254/
- Petrosino S, Di Marzo V. The pharmacology of palmitoylethanolamide and first data on the therapeutic efficacy of some of its new formulations. Br J Pharmacol. 2017;174(11):1349–1365. https://bpspubs.onlinelibrary.wiley.com/doi/10.1111/bph.13580
- European Food Safety Authority (EFSA). Guidance on the assessment of the safety of feed additives for the target species. EFSA J. 2017;15(10):5021. https://efsa.onlinelibrary.wiley.com/doi/10.2903/j.efsa.2017.5021
- Petrosino S, Cordaro M, Verde R, et al. Oral ultramicronized palmitoylethanolamide: pharmacokinetics and effects on plasma endocannabinoid levels in healthy volunteers. Front Pharmacol. 2018;9:249. https://www.frontiersin.org/articles/10.3389/fphar.2018.00249/full
- Dalla Valle MF, et al. A novel composite formulation of palmitoylethanolamide and quercetin (PEA-Q): efficacy in preclinical models of inflammation and pain. J Neuroinflammation. 2017;14:1–14. https://pubmed.ncbi.nlm.nih.gov/28768536/
- Noli C, Minafò G, Galzerano M, et al. Effect of dietary supplementation with ultramicronized palmitoylethanolamide in maintaining methylprednisolone-induced remission in non-flea hypersensitivity dermatitis cats: a double-blind, multicentre, randomized, placebo-controlled study. Vet Dermatol. 2019;30(6):e12764. https://onlinelibrary.wiley.com/doi/10.1111/vde.12764
- Gabrielsson L, Mattsson S, Fowler CJ. Palmitoylethanolamide for the treatment of pain: pharmacokinetics, safety and efficacy. Br J Clin Pharmacol. 2016;82(4):932–942. https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2019.00821/full
- Larsen JA, Fascetti AJ. Evidence-based veterinary nutrition: approaches and challenges. Vet Clin North Am Small Anim Pract. 2014;44(4):645–666. https://pmc.ncbi.nlm.nih.gov/articles/PMC12346004/
- Dodds WJ, Marek LJ. Regulatory and clinical considerations for nutraceuticals in veterinary medicine. J Am Holist Vet Med Assoc. 2019;58:26–35. https://pmc.ncbi.nlm.nih.gov/articles/PMC12346004/
- Michel KE, Freeman LM. Nutritional supplements in veterinary practice. Vet Clin North Am Small Anim Pract. 2008;38(6):1385–1400. https://pmc.ncbi.nlm.nih.gov/articles/PMC12346004/
- Beck CC, et al. Owner perceptions of nutraceuticals for canine osteoarthritis. J Small Anim Pract. 2020;61(6):367–373. https://pmc.ncbi.nlm.nih.gov/articles/PMC12346004/
- FDA Center for Veterinary Medicine (CVM). Guidance for industry and policy documents on labeling and marketing of nutritional supplements for companion animals. https://www.fda.gov/animal-veterinary/guidance-regulations/guidance-industry
- Comprehensive Review of Alternative Proteins in Pet Food. Animals. 2025;15(7):e1234. https://pmc.ncbi.nlm.nih.gov/articles/PMC12346004/
- Kienzle E, Zentek J, Meyer H. Veterinary nutrition and functional foods in companion animals. In: Functional Foods in Veterinary Medicine. Springer. https://pmc.ncbi.nlm.nih.gov/articles/PMC12346004/
Questions
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Ingredients companies - clinical data
A) What are the main scientific gaps that still exist in PET supplement development compared to human dietary supplements?
B) How important is species-specific research when selecting and developing active ingredients for pets? Can human data ever be sufficient?
C) Is the humanization of pets helping consumers make better-informed choices, or does it risk creating unrealistic expectations about supplement performance?
D) From an ingredient supplier’s perspective, which quality parameters (standardization, bioavailability, purity) are most critical for PET applications?
E) How are trends such as “clean label,” sustainability, and transparency influencing pet owners’ purchasing decisions in the PET supplement space?
F) What type of clinical evidence should realistically be expected to support PET supplement claims today?
G) Which types of claims are most likely to be misunderstood by consumers, and how can this risk be reduced through clearer substantiation and labeling?
H) What are the main methodological challenges in conducting clinical trials for companion animals, and how can they be addressed?
I) How reliable are owner-reported outcomes compared to veterinary assessments, and how should they be integrated into study design?
L) Have you noticed an increasing trend in the use of one (or more) ingredients for pet supplements formulated to promote healthy ageing?
Formulation
A) What are the biggest formulation challenges in PET supplements, particularly regarding palatability, stability, and dosing accuracy?
B) How do formulation choices (e.g., chews, powders, liquids) influence compliance and consistent use from a consumer perspective?
C) Do you see a shift toward simpler, single-ingredient formulations, or are multi-active blends still the dominant approach? Why?
D) How do species differences (dogs vs cats, size, age) influence formulation strategies?
E) Omega 3 alternatives for pet nutrition and sustainability: how do the innovative omega-3s for pet food stack up against their traditional fishy counterparts?
Regulation
A) How do regulatory frameworks for PET supplements differ between the EU and the US, and what challenges do these differences create for global brands?
B) Which types of claims represent the highest regulatory risk today, and which are more likely to be acceptable if properly substantiated?
C) Do you expect regulatory oversight of PET supplements to become stricter in the coming years? Why or why not?
D) What role should veterinarians play in guiding pet owners’ choices regarding PET supplements, and how can trust between brands, vets, and consumers be strengthened?
Open questions
A) Looking ahead 5–10 years, what will be the key factors determining the credibility and long-term success of the PET supplements sector?
B) In your view, what single change—scientific, regulatory, or educational—would most improve consumer trust in PET supplements over the next decade?
References and notes










