Help and FAQ

PhytoForm AI is a formulation engine and regulatory workspace for phytogenic feed-additive exporters. From a species, a functional goal and your export markets it ranks candidates from a registry of 600+ botanicals, proposes three blends with a lead assessment, returns a standard formulation with a projected COA, resolves the regulatory requirements of your target markets, assembles dossiers, generates manufacturing blueprints and scans claims for risk.

Formulators, regulatory affairs and QA teams, and founders at feed-additive companies that export phytogenic products: essential oils, botanical extracts, herbal preparations and their carriers. It is written from the exporter's side of the table.

After signing up and buying the trial pack, go to Dashboard, then New Formulation. Choose the species, one or more functional domains (for example gut health or heat stress) and your export markets, then run discovery. The engine returns three candidate blends, each with a lead assessment, in under a minute.

Poultry (broiler, layer, breeder), swine (starter, grower, finisher, sow), ruminants (dairy, beef, calf, goat, sheep), aquaculture (shrimp, fish), equine and companion animals (canine, feline).

A lead assessment is the score card attached to every candidate blend. It rates mechanism diversity (how many distinct modes of action the blend covers), novelty against known commercial products, evidence grade of the underlying literature, regulatory path in your chosen markets, and supply risk of the botanicals. Together they give a readiness score and a verdict such as Lead, Benchmark or Me-too, so you can choose the blend worth developing.

A standard formulation is the complete, batch-ready recipe for a blend: the actives plus carrier, flow aid, antioxidant and encapsulation, each as % w/w, together with the recommended dose per tonne of feed. It is what a plant or contract manufacturer needs to make the product, and it is the basis for the projected COA.

The registry holds 600+ botanicals: Indian, Himalayan and marine entries plus curated literature entries. Each carries marker compounds, assay ranges and mapped mechanisms across 25+ functional domains including gut health, methane mitigation, coccidiosis, heat stress, udder health, layer persistency, antiviral and analgesia.

Each time you change inputs and regenerate, a new version is created. Versions are numbered sequentially and each keeps its own standard formulation, lead assessment, projected COA, lab results and blueprint, giving you a full development audit trail.

The COA engine works from the standard formulation by mass balance: each ingredient's marker-compound assay is multiplied by its inclusion, with carrier dilution and encapsulation losses accounted for. The output is a target value and an acceptance range for each marker analyte. If you have uploaded lab results, calibration factors from your own batches are applied.

Yes. On any formulation version, open the COA and Lab tab and enter your measured values. The engine calculates the deviation for each analyte, shows whether the result sits inside the acceptance range, and uses it to calibrate future projections for that formulation.

Regulatory requirements can be resolved for 175 export markets. Named frameworks include the EU (Regulation 1831/2003), United States, United Kingdom, Canada, Australia, the GCC (Saudi Arabia, UAE and neighbours), China, Japan and Brazil; any other country is resolved through the framework it follows. Each lookup returns ingredient status, contaminant limits, labelling rules and the registration route, with sources.

Paste a label claim, marketing sentence or dossier passage, choose the document type and target markets. The scanner rates each phrase as high, medium or low risk for every market, explains the rule behind the rating, and proposes compliant alternative wording.

No. PhytoForm provides sourced regulatory summaries and claim risk assessments so you find problems early. Every regulatory output carries a reminder to confirm findings with a local regulatory consultant or the authority before submission.

A production sequence with parameters (temperatures, mixing times, speeds), critical control point flags for steps that affect safety or quality, in-process QC checks and equipment notes. Blueprints are generated per formulation version and can be downloaded as PDF.

Market-specific dossier sections built from your formulation data: identity and characterisation, projected specifications, safety and efficacy summaries, labelling and registration checklists in the structure the target authority expects, with completeness tracking. Technical data sheets and compliance summaries are also available.

Credits are consumed only when the engine generates something. A discovery and formulation run costs 2 credits, a projected COA 1, a regulatory refresh 2 per market, a claim scan 1 per market, a manufacturing blueprint 2, a dossier or document 2 each, and a lab-result calibration 1. Viewing, browsing and file uploads are free. There are no free credits: new accounts buy a one-time 50-credit trial pack (₹6,000 / $75); Professional and Business subscriptions add monthly credits.

Yes. One-time credit packs of 50, 100 and 250 credits are available on the plans page. Subscriptions give a better per-credit rate and a monthly allowance.