Quality & compliance

This is how we
manufacture.

Every product that leaves our facility is backed by the documentation a serious brand needs to list, sell and export.

Our position

Weak manufacturers hide behind packaging. We don't.

The compliance page most beauty manufacturers don't want you to read clearly is also the page that disqualifies most of them.

Every product we formulate and manufacture comes with the document stack needed for NAFDAC registration, retail listing and EU/UK export compliance.

Compliance framework

Three pillars. Every product.

01

GMP Manufacturing

Our Mile 2 facility operates under GMP protocols for batch control, equipment hygiene, raw material traceability and personnel standards.

Consistent product quality across batches. Documentation your retailer or export partner can actually use.
02

NAFDAC Registration Support

We produce the label input document, MSDS/SDS and INCI ingredient list your application needs.

You arrive at NAFDAC submission with a complete document pack, not a guessing game.
03

EU & UK Export Documentation

For brands targeting international distribution, CPSR documentation and INCI-compliant labelling are available on request.

A credible path to CPNP notification and UK Responsible Person registration.
Documentation standard

What every product
comes with.

This is the document stack included with every OEM or private label product we manufacture.

* CPSR available on request for Route B and C. Efficacy and stability testing available as an optional add-on for any route.

πŸ“‹

Product Specification Sheet

Full formula specification, ingredient grades, concentrations and batch reference.

🏷️

NAFDAC Label Input Document

Formatted label data per NAFDAC guidance, ready for your designer and submission.

⚠️

MSDS / SDS

Required by most retailers, export partners and logistics companies.

🌍

CPSR (on request)

Cosmetic Product Safety Report formatted for EU/UK compliance.

πŸ”¬

Stability Testing

Accelerated and real-time stability data confirming shelf life and expected storage performance.

βœ…

Claims Testing

Substantiation documentation for functional claims on your label.

πŸ“¦

Packaging Compatibility Sign-off

Confirmation that the formula is stable and safe in your chosen container.

πŸ“„

Label Review

A review of final label artwork against the approved label input document before print.

πŸ’Š

Efficacy Testing (optional)

In-use or in-vitro testing for premium or export-facing products.

Sampling policy

Paid sampling. Two revision rounds. No ambiguity.

Sampling fees are paid and non-refundable. Packaging must be confirmed before formulation begins.

Ready?

Start with a brief.
We handle the rest.

Category, route, target market, expected volume. That's all we need to begin.