Growth Guys Canada submits products to Janoshik Analytical — an independent, internationally recognized third-party laboratory — for comprehensive testing. The reports on this page are from Retatrutide Batch RET23, tested June–July 2026, and represent the standard of documentation Growth Guys provides across its product catalog.
Testing covers three independent methods: a blind identity test (confirming what the product actually is), HPLC purity analysis (measuring purity percentage across multiple vials), and an endotoxin safety report (testing for bacterial toxins). Very few Canadian peptide vendors provide all three.
Confirms the product is what the label says it is. Conducted blind — the lab doesn't know what it's receiving.
Measures the percentage of the target compound vs impurities. Multiple vials tested from the same batch for consistency.
Tests for bacterial endotoxins that can cause serious reactions. Measured in EU/Vial — lower is safer. Rare among Canadian vendors.
Task #200510 · Testing ordered Jun 26 '26 · Analysis conducted Jun 29, 2026 · Retatrutide Batch RET23 · Verify: QF96WVK2V1NW

Verify independently at verify.janoshik.com using key: QF96WVK2V1NW
A blind test means the laboratory receives the sample without being told what it is. The lab independently identifies the compound using mass spectrometry and chromatography, then reports what they found. This eliminates any possibility of confirmation bias.
For this test, Janoshik ran a Common GLP-1 peptide blind test — a panel capable of distinguishing between Semaglutide, Tirzepatide, and Retatrutide. The lab confirmed the sample is Retatrutide, exactly as labelled.
✅ Identity confirmed. Product is correctly labelled as Retatrutide. All three vials tested above 99.5% purity. This is pharmaceutical research grade.
Shimadzu LabSolutions · July 9, 2026 · Retatrutide Vial 2-30 · Batch 25370-3

HPLC (High-Performance Liquid Chromatography) is the gold standard analytical method for measuring peptide purity. A sample is injected into a column packed with a stationary phase. As the sample moves through the column, different compounds separate based on their chemical properties. A detector records each compound as it exits, producing the chromatogram (the graph you see in the report).
The peak table shows each detected compound, its retention time, concentration, and percentage of the total area. A single dominant peak with minimal surrounding peaks indicates high purity.
✅ Single dominant peak confirms product identity. 99.759% purity — well above the 98% threshold considered high-purity in research settings.
Shimadzu LabSolutions · July 9, 2026 · Retatrutide Vial 2-31 · Batch 25370-3

Testing a single vial only confirms that one specific unit meets quality standards. Multi-vial testing — running HPLC on multiple separate vials from the same batch — confirms that quality is consistent across the entire production run. This is a significantly higher standard than single-sample testing.
Vial B is the second of three independent vials tested from Batch 25370-3. Results closely mirror Vial A, confirming batch-wide consistency.
✅ Consistent with Vial A. 99.653% purity confirms batch-wide quality is not limited to a single cherry-picked sample.
Shimadzu LabSolutions · July 9, 2026 · Retatrutide Vial 2-32 · Batch 25370-3

Vial C is the third and final independent vial tested from this batch. Three separate vials, three separate HPLC runs, all conducted on the same day. Each vial is treated as a completely independent sample — there is no averaging or combining of results.
The consistency across all three vials (99.759%, 99.653%, 99.654%) demonstrates that this is not a one-off result — it reflects the true quality of the entire batch.
✅ Three vials. Three tests. All above 99.6% purity. Batch-wide consistency confirmed across the entire production run.
Task #200511 · Testing ordered Jun 26 '26 · Analysis conducted Jun 30, 2026 · Retatrutide Batch RET23 · Verify: QZHZ862WR1RN

Verify independently at verify.janoshik.com using key: QZHZ862WR1RN
Endotoxins are toxic molecules found in the outer membrane of certain bacteria (gram-negative bacteria). They are released when bacteria die and can survive standard sterilization processes including heat and filtration. Even in the absence of live bacteria, endotoxins can trigger serious inflammatory responses.
Endotoxin levels are measured in EU/Vial (Endotoxin Units per Vial). The lower the number, the safer the product. The test limit for this analysis was 10 EU/Vial.
Most Canadian peptide vendors do not provide endotoxin reports. Growth Guys does — making this one of the most complete testing packages available in the Canadian market.
✅ 1.911 EU/Vial — well within the 10 EU/Vial measurement limit. Endotoxin levels are low and acceptable for research use. This test is rarely provided by Canadian vendors.
Retatrutide Batch RET23 · Growth Guys Canada · June–July 2026
What this means
Five independent tests across three different methodologies all confirm the same conclusion: this batch of Retatrutide from Growth Guys Canada is correctly identified, consistently pure above 99.5%, and free of concerning endotoxin levels. The combination of blind identity testing, multi-vial HPLC purity analysis, and endotoxin safety testing represents a level of documentation that is uncommon in the Canadian peptide market.
Testing documentation is provided by Growth Guys Canada and conducted by Janoshik Analytical and Shimadzu LabSolutions. Reports shown are from Retatrutide Batch RET23, tested June–July 2026. Testing practices may vary by product and batch. This page is for informational purposes only and does not constitute medical advice.
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