Where supplements operations
break down.
Audit anxiety from incomplete records
Paper binders and spreadsheet batch records are difficult to search, easy to lose, and nearly impossible to produce quickly during an FDA or NSF audit.
Potency variance and label claim risk
Manual potency calculations create recalculation errors that put label claims at risk — and overages silently erode margins on every batch.
COA management across dozens of ingredients
Tracking Certificates of Analysis for every lot of every ingredient — and proving you verified them before use — is a full-time job when done manually.
Built for the way
supplements operators actually work.
Audit-ready batch records in minutes
Electronic batch records capture every step, signature, and timestamp automatically. When an auditor arrives, your documentation is complete and instantly retrievable.
Potency-based scaling from COA data
Our platform adjusts ingredient quantities based on actual assay values — so your label claims stay accurate without manual recalculation on every production run.
Lot-level COA tracking and verification
Every ingredient lot is linked to its COA, supplier, expiry date, and usage history. You can prove what you used, when you used it, and that it was verified before production.
GMP-compatible operator and training workflows
Operator qualification records, training matrix tracking, and role-based access controls keep your team compliant with GMP personnel requirements automatically.
Supplements businesses running
on our platform.
From small-batch producers to growing brands — regulated supplements manufacturers use our platform to run compliant, traceable, and efficient operations.
[PLACEHOLDER — Add testimonials and real customer logos here when available]
What this looks like
in practice.
Log incoming lot, attach COA, verify potency against spec before quarantine release.
System checks inventory availability, applies potency-based scaling from COA data, confirms operator qualifications.
Operators follow structured electronic batch record. Each step requires confirmation and e-signature.
QA reviews batch record, logs any deviations, generates COA with cryptographic verification for finished goods.
Run forward or backward trace on any ingredient lot or finished batch in seconds — not hours.
GMP and FDA requirements built into every workflow.
Our platform is designed to align with 21 CFR Part 11 electronic record and signature requirements. Audit trails are immutable, timestamped, and cryptographically chained. Batch records meet GMP documentation expectations without requiring paper binders or manual compilation.
Explore the tools built for your needs.
Our platform also serves:
CPG Operations
Setup Checklist
Know exactly what needs to be in place before implementing any system. A practical checklist for CPG operators starting from scratch or switching platforms.
[PLACEHOLDER — PDF checklist to be uploaded when finalized. Form currently sends inquiry to growth@cpgmpartners.com]
Get the Free Checklist
Full name and email required. No spam — ever.
Have questions before you start?
We're happy to help. Reach us directly at growth@cpgmpartners.com