Quality Assurance

Every Batch
Tested.
Every Time.

We don't ask you to trust our word. Every Supreme Labs product is independently verified by a certified third-party laboratory before it reaches you.

100%

Batches Tested

3rd Party

Independent Lab

6 Panel

Tests Per Batch

0

Failed Batches Released

The Process

From Manufacturing to Your Door

01

Raw Material Sourcing

We source only pharmaceutical-grade raw materials from verified, certified suppliers. Every ingredient arrives with documentation confirming origin and initial purity.

02

GMP Manufacturing

Products are manufactured in facilities operating under strict Good Manufacturing Practice (GMP) standards. Clean rooms, calibrated equipment, and documented procedures at every step.

03

Batch Sampling

Once production is complete, samples are taken from multiple points within the batch. This ensures the test results represent the entire production run — not just one portion.

04

Independent Lab Analysis

Samples are sent to an accredited, independent third-party laboratory with no commercial relationship to Supreme Labs. Results are unbiased and cannot be influenced by us.

05

COA Issued & Published

Once the lab confirms purity, potency and safety — a Certificate of Analysis is issued. We publish every COA here so you can verify the exact product you receive.

Our Laboratory

Certified.
Accredited.
Independent.

All Supreme Labs products are tested by an ISO/IEC 17025 accredited third-party laboratory. This accreditation is the international benchmark for testing and calibration laboratories — meaning results are globally recognised and technically sound.

Our laboratory partner has no financial interest in Supreme Labs and is selected specifically for their independence. They report to us — and to you — without any influence on the outcome.

Accreditation

ISO/IEC 17025

Testing Method

HPLC & MS

Turnaround

5 – 10 Days

Relationship

100% Independent

Lab Certification

Third-Party Verified

Identity ConfirmationPass
Purity ≥ 98%Pass
Heavy MetalsPass
Microbial SafetyPass
Solvent ResidualsPass
Release AuthorisationApproved

Frequency

When We Test

Every New Batch

Without exception. No batch is approved for sale before the COA is received and reviewed.

New Suppliers

When we onboard a new raw material supplier, their materials are tested before being approved for production.

Formula Changes

Any change to a product's formula or manufacturing process triggers a full new round of testing before relaunch.

Quality Control

Six-Panel Testing Protocol

Every batch must pass six independent tests before it is approved for release. A single fail means the entire batch is rejected.

Identity Testing

HPLC and mass spectrometry confirm the compound is exactly what it claims to be.

Required to pass

Purity & Potency

Active compound percentage verified to confirm correct dose in every unit.

Required to pass

Heavy Metals Screen

ICP-MS analysis checks for lead, arsenic, cadmium, and mercury contamination.

Required to pass

Microbial Safety

Tests for bacterial contamination, yeast, mould, and pathogens before release.

Required to pass

Solvent Residuals

GC analysis ensures no harmful residual solvents remain from the manufacturing process.

Required to pass

Release Hold

No product ships until the COA is received and reviewed. If it fails — it's destroyed.

Required to pass

COA Archive

Download Lab Reports

Every product with a Certificate of Analysis is listed below. Search by product name and download the PDF directly.

COAs will appear here once uploaded to products.

Transparency

Any Questions About Our Testing?

Our team is available on WhatsApp to answer anything about our products, testing or ingredients.