Independent Lab Testing
Every product batch we sell is independently tested by accredited third-party laboratories. No guesswork. No trust required — just verified data.
Why We Test Every Batch
The anabolic steroid market is rife with underdosed, mislabelled, and contaminated products. Studies published in peer-reviewed journals consistently find that a significant proportion of anabolic steroids purchased from online sources are incorrectly dosed or adulterated. We test every batch we receive precisely because we will not pass that risk on to our customers.
Our Testing Process
Batch Receipt
When a new batch arrives at our warehouse, samples are immediately pulled from multiple vials or blister packs across the batch for testing. No product enters our inventory before testing is initiated.
Sample Submission
Samples are submitted under blind reference numbers to our independent laboratory partners. No commercial information is shared with the lab to prevent bias.
HPLC & MS Analysis
High-Performance Liquid Chromatography (HPLC) is used to confirm concentration accuracy. Mass Spectrometry (MS) confirms compound identity. Results typically returned within 3–5 business days.
COA Publication
Passing batches receive a Certificate of Analysis (COA) which we publish on this page. Products that fail testing are rejected and destroyed — they never enter our inventory.
Ongoing Monitoring
We retest products from the same manufacturer after every major batch change. Consistency across batches is as important as a single passing result.
What We Test For
| Test Parameter | Method | Acceptable Result |
|---|---|---|
| Active compound identity | HPLC-MS | Compound confirmed as labelled |
| Concentration accuracy | HPLC-UV | Within ±10% of stated dose |
| Sterility (injectables) | USP <71> | No viable microorganisms |
| Bacterial endotoxins (injectables) | LAL Test | Below 0.25 EU/mL |
| Heavy metals | ICP-MS | Below WHO safe limits |
| Residual solvents | GC-Headspace | Below ICH Q3C limits |
| Related substances | HPLC | Below 0.1% individual impurity |
Certificate of Analysis Documents
Our laboratory partners are UKAS-accredited analytical testing facilities operating under ISO/IEC 17025:2017 standards. Accreditation details are printed on every COA document we publish.
Our Pass/Fail Standard
✓ PASS criteria
- Compound identity confirmed by MS
- Concentration within ±10% of label claim
- Sterility confirmed (injectables)
- Endotoxin below limit (injectables)
- No heavy metals above WHO thresholds
- No unexpected compounds detected
✗ FAIL — Product Rejected
- Wrong compound detected
- Concentration more than 10% outside label claim
- Any sterility failure
- Endotoxin above limit
- Heavy metal contamination above safe thresholds
- Unexpected active compounds detected
Quality You Can Verify
Every product we sell has a published COA. Browse our shop and check the lab results before you buy.
