ERRA
ERRA is a governed product-record system for US supplement brands and contract manufacturers, replacing spreadsheets and binders with a single source of truth for formulas, suppliers, batches, and quality records. The platform automatically derives Supplement Facts panels with rounding cited to 21 CFR 101.36 and prices every serving, while keeping an audit-ready trail for FDA inspections, retail buyers, and recalls. It also ties production records to exact formula versions and supplier lots, so a recall becomes a query rather than a war room.
- Artificial Intelligence
- Healthcare Technology
- Regulatory & Compliance Technology
- Software Only
Funding
Founders
Product
Problem
US supplement brands and contract manufacturers rely on spreadsheets, binders, and institutional knowledge to track formulas, batches, and quality records. When the FDA asks for formula history, a retail buyer requests approval records, or a reformulation drifts out of sync with the label, teams are forced into time-consuming file archaeology instead of pulling a single, reliable answer.
Solution
ERRA provides a governed product-record system that holds formulas, suppliers, batches, and quality records in one place cached by an unbroken chain of six modules. Users enter a formula once, and ERRA automatically derives the Supplement Facts panel with rounding cited to 21 CFR 101.36, prices every serving, and versions each change for full traceability. The platform also attaches supplier specs and certificates to lots, with confidence ratings that flag untrusted inputs. Testing requirements and results block batch release when needed, while production records are tied to the exact formula versions and supplier lots used, creating a trail that survives audits without the brand team in the room.
Target Audience
Primary users are US supplement brands and the contract manufacturers (co-mans) who produce their batches, including quality managers, regulatory affairs teams, and operations leads who need audit-ready records.
Features
- Versioned formulas with full history, costed servings, and Supplement Facts panels automatically rendered from the approved record with rounding cited to 21 CFR 101.36
- Supplier and specification management with certificates attached to lots and a confidence rating per ingredient input
- Batch testing module that tracks requirements, results, and approvals, with release block when tests do not pass
- Production records linked to exact formula versions and supplier lots, not to what a binder may say
- Fulfillment system integration (built, opening by invitation) that connects shipping data to the same record chain so recalls are executed as queries
- Six-module architecture that covers ingredients, suppliers, batches, production, records, and fulfillment in one governed system