Medical nutrition companies
Adding a format to an existing range, or taking a product from powder into a ready-to-consume pack.
Therapeutic application
Recovery nutrition is a guideline-driven category, and the guidelines have moved. Building a product here means knowing which recommendations are strong, which were recently downgraded, and which populations the evidence actually covers — because that decides both the formulation and what the pack is allowed to say.
The nutritional brief
Current perioperative guidance separates cleanly into recommendations that are strong and cost nothing, and recommendations that are weak and involve buying something. An honest product page should say which is which.
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.
Clear, low-osmolality maltodextrin drinks built to empty from the stomach inside the fasting window.
Develop a pre-op drinkPost-operative and convalescent supplements delivering protein and energy in a small serve.
Develop an ONSArginine, omega-3 and nucleotide formats for the perioperative populations the evidence covers.
Develop an immunonutrition formatReady-to-eat meals carrying the protein and energy density a catabolic state needs.
Develop a recovery mealGentle textures for the early days after surgery, when appetite and tolerance are both low.
Develop a soft formatPortion-standardised formats for inpatient use and for the weeks after discharge.
Develop a hospital 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 is still a real category with a live specification, but the claim has to be current. The 2025 ERAS colorectal guideline rates it weak and says it offers no advantage in comfort or clinical outcomes over a standard short fast, while ESPEN still recommends it. We will help you build the product and we will tell you what the label can defensibly say, which is narrower than it was five years ago.
Because it has to be clear and empty from the stomach inside the fasting window. Protein and fat both delay gastric emptying, so they are excluded. Near-isotonic, carbohydrate only, no fat, no fibre — the formulation looks simple because the envelope is that tight.
No. The highest grade we can verify in current guidance is Grade B, for perioperative arginine, omega-3 and nucleotide formulas in major tumour surgery. Some recent independent trials have failed to reproduce earlier positive findings. We would rather you had a product that holds up than a claim that does not.
It needs one in practice. Arginine-supplemented diets are not recommended in severe sepsis or critical illness, and the intended population has to be stated on the pack. This is one of the places where a precaution belongs on the front of the file rather than the back.
Only if the position is repletion. The current Cochrane review finds insufficient evidence for zinc and vitamin C in pressure ulcer prevention and treatment, and mixed evidence for the arginine combination. The mechanisms are textbook; the trial evidence is not there. Adequate protein and energy is the part you can stand behind.
It depends on the market and on the classification. In the European Union a food for special medical purposes cannot carry nutrition or health claims at all — it communicates through its intended-use statement. In India, the condition statement on a food for special medical purpose is subject to approval by the Authority on scientific and clinical evidence. We scope that with you before the formulation is fixed, not 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.