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. Formulas you import keep their prior approval, clearly marked as imported. Adopting one runs it through ERRA's release gate, after which it is tracked like any approval decided in ERRA.
- 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
It starts with a record that can be checked.
Recorded and shared through ERRA.