ERRA for R&D
Build and iterate on a formula with the panel, cost, and compliance checks attached, not bolted on after.
What you do in ERRA
You build the formula: ingredients, amounts, overage, flavor variants, proprietary blends. You create trial versions, iterate, and promote a version to production when it is ready. Once a version is approved, it is locked; the next iteration is a new version, so your working history is never overwritten.
You see the Supplement Facts panel and cost-per-serving update as you formulate, instead of waiting for a separate label pass to catch a problem.
What ERRA gives you
- Immutable formula versions with comparison, so you can see exactly what changed between iterations.
- Deterministic panel and cost-per-serving calculation as you formulate, not after.
- Allergen, dietary-flag, Prop 65, and upper-limit checks derived from the formula automatically.
- A release-readiness gate that names the specific blocker before you take a version to Quality Assurance, instead of a rejection with no reason. Formula versions created by the historical bulk importer arrived pre-approved as part of that migration and were never run through this gate.
- A brief-to-handoff workspace rail that keeps the product-development stages on one page.
Where the record hands off
When a version is ready, Quality Assurance reviews it against the same release-readiness gate you already saw. Procurement and Quality Control work off the supplier and ingredient facts you connected. Nobody downstream is re-keying your formula.
Keep reading
Continuous attestation starts with a record that can be checked.
They check the sample. We attest to the system.