- Mag Prime Labs
- Not provided
- Not provided
- Not provided
This certificate was shared with the named partner at the submitting customer's request. Sharing does not establish the partner's identity, the product's origin, or the partner's authorization of the test.
- L1Identity
- L2Purity
- L3Net Peptide Content
- L4Sterility
- L5Bacterial endotoxin, USP <85> (kinetic chromogenic LAL)
- L6Heavy Metals
- L8Fentanyl Screen
More views of Vial A
Test Results
Select a test for its full result| Test | Specification | Result | Verdict |
|---|---|---|---|
research screen | Specificationevery vial within ±1 Da of 4731.421 Da | Result4731.445 Da | PASS |
research screen | Specification≥ 99.25 area % | Result99.91% | PASS |
research screen | Specificationevery vial within ±10% of 10 mg | ResultVial A: 10.58 mg | PASS |
research screen | SpecificationRapid PCR screen | ResultTarget DNA not detected | PASS |
verified compendial | Specification≤ 0.5 EU/mg (house limit; USP <85> method) | Result0.197 EU/mg | PASS |
research screen | SpecificationICH Q3D(R2) Table A.2.2, parenteral route | ResultAll below limits | PASS |
research screen | Specificationno fentanyl or analog at or above 1 ng/mg | Resultnone detected | PASS |
SUPPORTING GRAPHICS
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.
- [Fentanyl Screen]Targeted LC-MS/MS adulterant screen, reported as detected or not detected against its stated detection limit. A harm-reduction research screen, not an exhaustive adulterant panel.
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.
To the maximum extent permitted by applicable law, the cumulative liability of Axiom Analytics, its officers, employees, and third-party laboratory partners to the client or any third party for any claims, losses, damages, or liabilities of any kind (including but not limited to direct, indirect, special, incidental, punitive, or consequential damages) shall be strictly limited to, and shall not exceed, the exact dollar amount paid by the client to Axiom Analytics for the specific individual analytical test run from which the liability arose.