Lab Reports

Current OROS batches undergo independent third-party testing before release. The testing documented for each lot is identified on its product page and corresponding entry in our COA Library so researchers can evaluate the evidence for the specific batch they are purchasing.

Up to 12 points of testing, including heavy metals, sterility, residual solvents, and adulterants.  The full 12-point panel is intended for vials. Solvents, topicals, research sprays, capsules and other formats have their own applicable testing panels. Completed testing varies by product and batch; consult the published report for your lot.

Independent laboratories may hold ISO/IEC 17025 accreditation for defined scopes. Accreditation applies only to the methods and activities listed within each laboratory's accredited scope and should not be interpreted as blanket accreditation of every test or product.

Up to 12 points of testing, including heavy metals, sterility, residual solvents, and adulterants.  The full 12-point panel is intended for vials. Solvents, topicals, research sprays, capsules and other formats have their own applicable testing panels. Completed testing varies by product and batch; consult the published report for your lot.

• Purity (HPLC)
• Identity (USP <621>)
• Net Content (HPLC)
• Multi-Vial Variance
• Endotoxins (USP <85>)
• Microbial (USP <61>/<62>)
• Heavy Metals (ICP-MS, USP <233>)
• Residual Solvents (USP <467>)
• Adulterant Testing (USP <2251>)
• Sterility (USP <71>)
• Solubility (USP General Notices 5.30)
• Container Closure Integrity (USP <1207>)

The current program includes separate sterility testing (USP <71>), solubility testing (USP General Notices 5.30), and container closure integrity testing (USP <1207>). Microbial and endotoxin tests are distinct from sterility testing. Only tests and results documented for the specific lot apply; the current program does not establish results for historical lots.

We believe quality claims should be supported by documentation. Batch-specific COAs and available laboratory records can be reviewed through individual product pages and our COA Library .

Researchers should not have to rely on vague statements, screenshots, or unverifiable testing claims when evaluating research materials.