Posted by OVRA
Every OVRA lot goes through the same sequence before it ships.
First, manufacturing in an FDA-registered, cGMP-compliant facility in the USA. cGMP — current Good Manufacturing Practice — is the FDA's standard for how supplements must be produced, documented, and controlled.
Second, independent testing. A third-party laboratory verifies identity (the ingredient is what the label says), potency (the dose is what the label says), and purity (contaminants, including heavy metals, are below limits).
Third, the paperwork. Each lot's results are recorded in a certificate of analysis. The COA for your lot is available on request — write to us with your lot number.
None of this is exciting, which is rather the point. Verification is quiet work. We would rather show you a document than an adjective.
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
