One request, followed end to end
The walkthrough below follows a broiler gut-health request for three export markets through every stage the engine handles, with the credit cost of each stage.
An exporter needs a broiler gut-health blend it can register in the EU, Saudi Arabia and Vietnam, with a formulation sheet, projected COA and batch instructions for a contract manufacturer.
About 19 credits
for the whole run, three markets included
You: You select broilers, the gut-health domain, and three export markets: EU, Saudi Arabia and Vietnam.
What the engine does
The engine loads the target mechanisms for the domain, the relevant marker compounds, and the regulatory constraints for the three markets before it looks at a single botanical.
Output: A scoped request. Nothing is charged yet.
You: You run discovery.
What the engine does
Candidates are ranked from a registry of 600+ botanicals by mechanism fit, evidence grade and supply. Three blends are composed, each with a lead assessment scoring mechanism diversity, novelty against known commercial products, evidence grade, regulatory path and supply risk.
Output: Three candidate blends, each with a lead verdict and readiness score.
You: You pick the lead blend.
What the engine does
The engine expands it into a standard formulation: actives plus carrier, flow aid, antioxidant and encapsulation, dosed per tonne of feed. It projects a COA specification for the marker compounds, for example carvacrol at 8.4% w/w with an acceptance range of 7.2 to 9.6%.
Output: Standard formulation sheet and projected COA, downloadable as PDF.
You: You open the regulatory view for the three markets.
What the engine does
Requirements are resolved per market: ingredient status, contaminant limits, labelling, registration route. The heatmap shows where the lead blend is clear, conditional or blocked, and the dossier compiler assembles the market-specific sections from the formulation data.
Output: Regulatory heatmap plus a dossier draft per market.
You: Marketing proposes the claim "prevents E. coli infection in broilers". You paste it and select the EU.
What the engine does
The scanner flags it as high risk: therapeutic claims for feed additives require veterinary medicinal authorisation in the EU. It proposes "supports intestinal microflora balance" as compliant wording.
Output: Risk flag, reason, and alternative phrasing.
You: You request the blueprint for a 500 kg batch.
What the engine does
The blueprint lists the mixing sequence, temperature limits, encapsulation step and critical control points, for example adding essential oils below 40 degrees C to avoid volatile loss, plus in-process QC checks.
Output: Batch instructions your plant or a contract manufacturer can follow.
You: The pilot batch returns from the lab with carvacrol at 8.1% w/w. You enter the result.
What the engine does
The engine records a deviation of about 3.6% from projection, confirms it is inside the acceptance range, and applies the calibration to future COA projections for this formulation.
Output: Deviation report and a tighter next COA.
The walkthrough covers one request. These apply to every project.
Every candidate carries a score for mechanism diversity, novelty, evidence grade, regulatory path and supply risk, so you can defend the choice to a buyer.
EU, US, UK, Canada, Australia, GCC, China, Japan, Brazil and any other country resolved by its regulatory framework.
Gut health, methane mitigation, coccidiosis, heat stress, udder health, layer persistency, antiviral, analgesia and more.
Each regeneration creates a new version with its own formulation, COA, lab results and blueprint.
The scenario above used about 19 credits. The 50-credit trial pack (₹6,000 / $75, one-time) covers two runs of that size. No subscription required.