1. Qualified Buyer Standard
Ourovia supplies licensed research institutions, contract research organisations, university laboratories, and independent research scientists. All accounts undergo institutional review prior to first shipment.
— Compliance
Research Compliance
Our compliance framework exists to keep Ourovia specimens inside legitimate research workflows — and out of unsanctioned hands.
Last Updated · May 2026
2. Chain-of-Custody
Every batch is documented from raw-material lot through synthesis, purification, lyophilization, third-party verification, and dispatch. Documentation is retained for seven years and made available on request to verified clients.
3. Prohibited Use
Ourovia specimens may not be administered to humans or animals under any circumstances.
Re-sale to consumers, unverified resellers, or anonymous parties is strictly forbidden and grounds for immediate account termination.
4. Third-Party Verification
Independent analytical laboratories (including Tanshi and Janoshik Analytical) verify every batch for HPLC purity, mass-spectrometry identity, and LAL endotoxin within published acceptance thresholds.
5. Reporting Concerns
Suspected misuse or counterfeit Ourovia material should be reported to compliance@ourovia.bio. All reports are reviewed confidentially.