Originated by The Peptide Collective, which attests it authorized this test as the brand of record.
Axiom confirmed this brand is a registered Axiom account. This does not confirm the product's origin, chain of custody, or that the brand authorized this specific test.
- L1Identity
- L2Chromatographic & Carrier Purity
- L3Declared Content
- L4Sterility
- L5Endotoxin
- L6Heavy Metals
- L7Physicochemical Properties
More views of Vial A
Test Results
Select a test for its full result| Test | Specification | Result | Verdict |
|---|---|---|---|
verified compendial | Specificationretention time corresponds to the reference standard run on the same sequence within the locked 2% window (Verification of GC-FID identity vs reference standard (USP <621>), gc_fid_identity v1.0, evidence82fefc99-4670-4c11-8106-2c19418fed64, sha25675e3a31f2390c360ae36830da424e6e53575de2782be9c4fc87039224fcdbd7d, /validationParameters/0/acceptanceCriterion: Sample RT within ±2.0% of the reference standard (USP <621> convention). Retained unchanged by gc_fid_identity v1.1, evidence28b7931f-3460-4db1-9e6a-f3911d84a01e, sha256d02d290b42521ec7193d40d9c5b207be889a9869ed6aa7e8a6baa2e2500c3258.) | Resultanalyte 6.18 min, reference standard 6.2 min | PASS |
verified compendial | Specificationat least 99.25% by GC area normalisation, largest single impurity at or below 0.3%, total impurities at or below 0.5% | Result99.41% GC area% (largest single impurity 0.15%, total impurities 0.25%) | PASS |
verified compendial | Specification80-120% of the frozen label claim; stored percentage must equal measured content / declared content × 100; USP <341> system suitability and traceability required | Result0.889592 % w/v · 98.8436% of the 0.9% w/v label claim | PASS |
research screen | SpecificationRapid PCR screen | ResultTarget DNA not detected | PASS |
verified compendial | Specification< 0.5 EU/mL (USP <85>) | Result0.005 EU/mL | PASS |
research screen | SpecificationICH Q3D(R2) Table A.2.2, parenteral route | ResultAll below limits | PASS |
research screen | SpecificationpH within 4.50 - 7.00 | ResultpH 4.86 | PASS |
research screen | Specificationcolorless; clear; free from visible particles | Resultcolorless; clear; no visible particles observed | PASS |
REPORTING SCOPE & LIMITATIONS
- [Sterility · Rapid PCR]Rapid PCR screen for microbial DNA. It detects DNA from live and dead organisms and is not a USP <71> sterility test or a USP <61> count. Full USP <71> sterility testing is available as an add-on.
Results relate only to the item or portion tested. Unless sampling was performed or witnessed by Axiom Analytics, the laboratory does not attest that the submitted sample represents the wider lot or batch. A PASS designation means only that the reported result met the specification shown. It does not establish safety, efficacy, regulatory approval, legality, or suitability for human or animal use.
All analytical testing, validation reports, and interactive Certificates of Analysis (COAs) provided by Axiom Analytics are intended strictly for Research Use Only (RUO) in in-vitro or laboratory animal model environments. Axiom Analytics does not analyze, validate, evaluate, or make any representations regarding the safety, efficacy, toxicity, or legality of any tested substance for human or animal consumption, veterinary use, clinical diagnostics, food additives, cosmetics, or household applications.
Testing is performed within Axiom's laboratory network under Axiom's methods. Every result is reviewed and released by Axiom, which issues and is responsible for this certificate. Axiom Analytics does not hold ISO/IEC 17025 accreditation. Samples are identified to the testing laboratory by an internal lot ID only. The method status of each result is shown beside it.
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