Formulation software where the approved recipe IS the batch.
Most formulation software stops at R&D — a tool to model BOM cost and ingredient ratios that then gets re-keyed into the MES, the ERP, or paper. V5 keeps the formula and the execution in one system: the formula you approve in the lab is the formula the operator works on the kiosk that night, with the e-signed change-control trail to prove it. No drift. No re-keying. No paper.
What changes once Formulation software is live.
Indicative ranges from V5 pilot deployments. Your numbers will land near these once the workflow is operator-led and e-signed at the step.
What changes the day you switch this on.
Manual, paper-driven, and only audited after the fact.
Tribal knowledge in spreadsheets and shared drives.
Errors caught at month-end — too late to fix the batch.
Different teams keep their own version of the truth.
Versioned master recipes
Per-strength / per-batch-size scaling
BOM cost, yield & margin modelling
Allergen, controlled-substance & potency flags
What you actually get
Operator-led, e-signed, immutable. Engineered for regulated manufacturers — not retrofitted.
Versioned master recipes
Every formula is versioned with effective dates, e-signed approval and a change-control trail. The active version drives every WO until you sign a new one in.
Per-strength / per-batch-size scaling
One master formula scales to any batch size with tolerances re-derived automatically. Density, moisture and overage are tracked per ingredient.
BOM cost, yield & margin modelling
Model ingredient cost, target yield, and finished-good margin before you release the formula — V5 carries the actuals into the post-batch yield report.
Allergen, controlled-substance & potency flags
Flag ingredients that drive cleaning validation, DEA controls or two-person dispense. The kiosk enforces the rule on every batch.
Compare formulas side-by-side
Diff two versions of a recipe — ingredient changes, tolerance changes, in-process checks added or removed — for change-control review and FDA / Notified-Body inspection.
ERP-extending
V5 reads BOM and recipe data from your ERP and pushes back actual consumption. Purchasing, finance and demand planning stay where they already are.
Curious how this lands in your environment?
One operator action — a complete, signed record.
What it leaves behind
- Formula version is what the kiosk runs — no re-keying
- Change-control + e-signature on every revision
- Per-batch-size scaling re-derives tolerances
- Allergen / potency flags enforce cleaning validation
- Free trial, no credit card, onboard in days
The clauses this satisfies
What buyers ask before they switch on Formulation software where the approved recipe IS the batch..
The rest of the platform this plugs into.
V5 isn't a bolt-on. Every module shares the same data, the same audit trail, the same operator. Pick where to look next.
MES
Operator-led execution: scan-gated dispense, step-by-step kiosk, equipment + scale integration, live yield. Built for regulated process & discrete manufacturing.
WMS
Receiving, putaway, transfers, cycle counts, picks, pack & ship — all lot-aware, bin-accurate, FEFO/FIFO-enforced and barcode-driven.
QMS
Built-in QMS: deviations, CAPA, supplier scorecards, in-process AQL, release-by-exception. Aligned with 21 CFR 211/820, ISO 13485 and 111.
Got questions, or want to see it on your shop floor?
Ask V5 — our code-aware assistant — or spin up a workspace. Both are free.