cGMP · 21 CFR Part 11 audit trail
Formulate, dispense, test and release pharmaceutical batches with the controls a regulated plant needs — quarantine isolation, FEFO picking, potency-adjusted scaling, yield reconciliation and a permanent record of every change.
Recipes with active potency adjustment, per-material loss and volatilization tolerances, and stage-by-stage instructions tied to equipment.
Scale any recipe to the batch size you need, then reconcile theoretical against actual output with automatic deviation alerts.
Every receipt lands in quarantine. Picking always proposes the earliest-expiring released lot, and surplus returns keep lot traceability.
Assay, moisture and physical results with Certificate of Analysis upload, then a signed release or rejection decision.
Who, when, what changed, old and new value, and the justification — written by the database and impossible to edit or delete.
Nine plant roles from Super Admin to Maintenance Engineer, each with its own dashboard and permissions.