Omni 8X Testing. Quality You Can Verify.
Omni’s eight-category testing program. Only lots with completed documentation are represented as 8X tested; consult the specific laboratory report for the tests and results available.
Reports identify the laboratory that performed the analysis. Review the original report for laboratory details, methods, results and the matching lot and strength. View COA's.
A purity percentage describes one property of the material. It says nothing about identity, content, or contamination.
Testing is performed by an outside laboratory, not by us. We publish what the report says — nothing more.
Results belong to a specific production lot and strength, and are published against that lot's certificate.
The Eight Tests.
Each category is a distinct part of the standard. Final names, methodology and specifications publish exactly as written on the ILS Laboratories reports.
Measures the proportion of the target compound in the tested sample.
Reported per lot (RP-HPLC, 214 nm)
Quantifies the actual amount of compound measured in the vial.
Reported per lot (mg)
Confirms the tested material matches the compound named on the label.
Confirmed per lot (HPLC-RTM)
Compares additional vials from the same lot for analytical consistency.
3 vials tested per lot
Screens the tested lot for five documented elemental contaminants.
ICP-MS per USP <233>
Checks the tested lot for detectable microbial growth.
PCR, no-growth specification
Measures bacterial endotoxin present in the tested material.
Quantitative result, USP <85>
Screens the tested lot for fentanyl at the laboratory's stated cutoff.
Immunoassay, 50 ng/mL cutoff
Results belong to a specific lot.
Every batch we release carries its own lot number, and every certificate we publish is tied to that lot and strength. A result from one batch is never presented as coverage for another. If a strength has no certificate yet, its card says so rather than borrowing a neighbouring result.
You can view the documentation for any lot through Omni's COA system — on the product page under Certificate of Analysis, or on the central COA page. Each completed 8X report attaches to the same lot record you already use, so nothing about how you verify a batch changes.
All Omni Research products are supplied strictly for laboratory research use only. Not for human consumption. Not for medical use.
