← Quality & Compliance Overview

Supplement Compliance Documentation

Most suppliers send the Certificate of Analysis, the specification sheet and the safety data after you ask — sometimes after you order. We publish ours up front, because a document you can read before the order is worth more than one promised during it.

What ships with every batch

Quality assurance archive with neat rows of identical plain ring binders

IN-HOUSE CAPABILITY

Compliance Vault and Quality Documentation

Every batch we release leaves a paper trail, and buyers increasingly want to see it before they place an order. This page sets out what we hold, what we can share under NDA and what is issued with each shipment.

  • Certificate of Analysis (COA) — every parameter we test, with the specification, the test method and the result for that specific batch
  • Material Safety Data Sheet (MSDS)
  • Specification sheet — the agreed description of the finished product
  • Nutritional panel
  • Allergen statement
  • Certificate of Origin
  • Health certificate

Additional documents required by your customs authority can be prepared on request.

Download two documents now

Both of these are available without a form and without a call. They show you what we test and what we check for, before you have committed to anything:

The COA template shows exactly which parameters we test and report, so you can check whether the panel matches what your market requires. The compliance checklist covers US FDA labelling and Amazon supplement requirements.

Certifications our facilities hold

  • HACCP — hazard analysis and critical control points across all production lines
  • ISO 22000 — food safety management system
  • cGMP — audited by SGS, governing facility hygiene and process control
  • HALAL — certified for Muslim-majority markets
  • US FDA Food Facility Registration — required for export to the United States

What each certificate covers, and how to verify it with the issuing body, is described on the certifications page.

Label and market review support

We review your label artwork against the requirements of your destination market and tell you what we would change — claim wording, allergen declaration format, net quantity statement, ingredient naming and order. We also support pre-shipment sample submission to your own third-party laboratory, so your own certificate and ours can be compared on the same batch.

What we do not do

We are a manufacturer, not a regulatory authority. We can tell you what a market requires and prepare the documentation to match it; we cannot approve a claim on your behalf, and final responsibility for the labelling and claims on a product sold under your brand rests with you. Where a market requires a notified registration or an in-country agent, we will say so clearly and support the process — we will not quietly ship around it.

Everything Under One Contract

Formulation

Your formula or target actives turned into a stable, manufacturable specification.

Manufacturing

Blending, encapsulation, compression, gummy depositing, powder and liquid filling.

Quality Control

In-process checks and finished-product release testing against the written spec.

Documentation

Batch records, a Certificate of Analysis and export paperwork with every shipment.

Request Our Documentation Pack

Tell us which certificates or records your buyer needs. We reply within 48 hours with what we can share and under what terms.

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