Medical nutrition companies
Adding a format to an existing range, or taking a product from powder into a ready-to-consume pack.
Therapeutic application
The commercial difficulty with sarcopenia is that the product has to carry a large protein dose in a small serve, for people who eat less. That combination sits almost exactly on the concentration where protein stops behaving under heat. The formulation problem and the manufacturing problem are the same problem.
The nutritional brief
Sarcopenia is defined by strength first and mass second. The nutritional brief that follows from that is about protein dose, protein quality and total intake — not about a single active.
What we develop
Each one is developed as its own product with its own specification — formulation, process and the analysis that proves the finished pack meets the profile it declares.
Ready-to-drink supplements carrying a full protein dose in a serve someone will finish.
Develop an ONSPuddings, creams and spoonables for people who manage a spoon better than a glass.
Develop a spoonableEveryday meals carrying a raised protein density, for people who will not drink a supplement.
Develop a fortified mealBlended plant systems built to close the amino acid gap rather than ignore it.
Develop a plant formatCombination formats where the micronutrient profile is declared and validated post-process.
Develop a combination productPortion-standardised products for care homes, hospitals and institutional supply.
Develop a clinical formatWhat we change
Formulating for this category is about choosing a system that arrives at the specification after processing and storage, rather than one that meets it in the kitchen.
Straight answers
We would rather you launched a product that holds up under scrutiny than one carrying a claim that does not. These are the places where the evidence is weaker than the category implies.
Who we develop for
Products in this category are developed here for the organisations that have to put them in front of a clinician, a procurement team or a regulator.
Adding a format to an existing range, or taking a product from powder into a ready-to-consume pack.
Moving from general wellness into a defined clinical need, where the profile becomes the specification.
Producing to a standardised portion and profile, centrally, and shipping ambient.
Supplementary and therapeutic feeding where composition, shelf life and cost per serve are fixed by tender.
Sourcing under your own brand, needing the formulation and process proven before a co-packer is committed.
Inside an established manufacturer, needing formulation, process and regulatory work in one place.
The technical side
If you are briefing an R&D, regulatory or quality team, or answering a tender or an importer’s questionnaire, these are the concepts the work is built on.
Related work: clinical nutrition, therapeutic nutrition, retort clinical and medical nutrition and clinical trial management.
Questions
It depends on how the protein system is built rather than on the number alone. Above roughly eight to ten per cent total protein you are in the band where uncontrolled whey aggregation causes thickening, sedimentation and later gelation. Raising the casein fraction and pre-denaturing the whey under controlled conditions both move that limit. A pilot establishes where your specific system sits.
For processing stability, a higher casein fraction is the friendlier system. For post-prandial response, whey digests faster. For cost, market and dietary positioning, plant systems may win, but they need blending to close the amino acid profile. We would rather work backwards from your market and your process than recommend one in the abstract.
Be careful. In people already eating enough protein, supplementation has not shown significant effects on lean mass, strength or performance, and it added nothing over resistance training alone. Where intake is genuinely low, repletion is a defensible position. What the label may say then depends on the market and the product's classification.
Sometimes, and more narrowly than the category suggests. Adding free leucine to a slow protein does augment the acute response, and practical guidance pairs a 25–30 g protein meal with a leucine content in that region. But the trigger hypothesis held in only 16 of 29 studies reviewed, and mostly with isolated protein sources at sub-maximal doses.
If you are adding it for falls, the evidence sits at 800–1000 IU daily, in populations that are deficient, on daily rather than intermittent dosing. Higher doses increased falls in the same analysis. That is an unusual dose-response and it should shape the format, not just the number.
Age gelation. Heat-treated high-protein liquids can gel weeks or months after production, and no release test catches it because it has not happened yet. Only a real-time stability programme finds it, which is why we run one before a launch rather than after.
See the wider applications index
Next step
Send the target profile, the format you have in mind and the market you are selling into. We will tell you what is achievable, what the evidence will and will not support on the label, and what the development work would need to cover.
Food Research Lab strives for excellence in new Food, Beverage and Nutraceutical Product Research and Development by offering cutting edge scientific analysis and expertise.