Supplement and nutraceutical manufacturing software
Complete lot tracking, digital batch records, and formula management for dietary supplement manufacturers. Supports FDA compliance and recall-readiness — without the complexity of enterprise ERP.
30-day money-back guarantee · Go live in 3–6 weeks
The challenges supplement manufacturers face
cGMP compliance requires complete batch records
FDA 21 CFR Part 111 requires batch production records for every supplement run — ingredients, quantities, operators, and test results. Most supplement manufacturers still track this on paper or in spreadsheets.
How Brahmin solves it
Digital batch records created automatically for every production run. Ingredient lot numbers, operator records, and yield data captured at the time of production — not reconstructed later.
A recall without traceability is a crisis
When the FDA issues a warning letter or a supplier calls about a contaminated ingredient, you need to know within minutes which customers received affected product. Without traceability, that can take days.
How Brahmin solves it
Full forward and backward lot traceability. In a recall scenario, Brahmin tells you exactly which customers received product from a specific ingredient lot — with a report ready to share in minutes.
Formula changes create compliance exposure
Changing a formula mid-production without proper documentation creates gaps in your compliance record. Which batches used the old formula? Which used the new one? Without version control, it's nearly impossible to answer.
How Brahmin solves it
Version-controlled formulas tied to every production run. Every batch record shows exactly which formula version was used, with full ingredient lot traceability.
Everything you need to run your supplement business
Lot & batch traceability
Full forward and backward traceability from raw ingredient to finished product. Recall reports in minutes.
Digital batch records
Automated batch production records with ingredient lots, operator data, and yield — created at time of production.
Expiration date management
Track ingredient and finished product expiration dates with FEFO picking and automatic alerts.
Certificate of analysis storage
Attach CoAs and supplier qualification documents directly to ingredient lot records.
Formula BOM management
Version-controlled formulas with exact ingredient quantities, substitutions, and true cost rollup per batch.
Supplier traceability
Track which supplier lots went into which finished batches. Know immediately when a supplier issue affects your product.
Common questions about Brahmin for supplement manufacturers
Does Brahmin Solutions support cGMP compliance for supplement manufacturers?
Brahmin supports the operational requirements of cGMP compliance under FDA 21 CFR Part 111 — including digital batch production records, lot traceability from ingredient receipt to finished product shipment, CoA document storage, and expiration date tracking. Brahmin is a manufacturing and inventory platform; cGMP certification requires a broader quality management program, which Brahmin supports but does not replace.
Can Brahmin track supplement lots and expiration dates?
Yes. Every ingredient received in Brahmin gets a lot number, an expiration date, and a supplier record. Every production batch is linked to the ingredient lots used. FEFO (first expired, first out) picking rules ensure you ship oldest-dated product first, and automatic alerts notify you before product approaches expiration.
How does Brahmin support FDA dietary supplement recordkeeping requirements?
Brahmin creates digital batch production records for every supplement production run, capturing ingredient lot numbers, quantities, operator information, and actual yield. These records are searchable and exportable, giving you the documentation foundation that FDA inspectors expect under 21 CFR Part 111.
Does Brahmin manage certificates of analysis for supplement manufacturers?
Yes. CoAs and other supplier qualification documents can be attached directly to ingredient lot records in Brahmin. When an auditor asks for the CoA for a specific lot, you can pull it up in seconds — not hunt through email folders.
Ready to simplify your supplement operations?
Join 300+ manufacturers who switched from spreadsheets to a single source of truth. Go live in 3–6 weeks with a dedicated implementation manager.
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