How Vigor Rise is made and checked
Vigor Rise is produced in an FDA-registered facility under current Good Manufacturing Practice, and every production batch is screened by an independent ISO/IEC 17025 laboratory before it ships. Quality is the process; the verification page shows the result for the current batch.
Where Vigor Rise is manufactured
Vigor Rise is manufactured in the United States in a facility that is registered with the FDA and follows cGMP standards. cGMP covers how raw materials are received and quarantined, how equipment is cleaned, how each step is documented, and how finished bottles are sealed and tracked. It is the same framework that lets a batch be traced from raw ingredient to the bottle in your hand.
What we test on every batch
- Identity. Confirming each botanical is what the label says, by HPLC and supplier documentation.
- Potency. Verifying the standardized actives, such as icariin and ginsenosides, meet the stated levels.
- Heavy metals. Screening for lead, arsenic, cadmium, and mercury by ICP-MS, with the current batch at < 0.6 ppm.
- Microbial safety. Testing for total counts and pathogens against USP limits; the current batch passes.
Our independent laboratory
Batch screening is performed by Brockwell Assay Group, LLC, an ISO/IEC 17025 accredited third-party laboratory. Using an outside lab matters because it removes the conflict of grading your own homework: the lab has no stake in the result, only in the accuracy of the test.
| Test | Result |
|---|---|
| Active purity (HPLC) | 99.2% |
| Heavy metals (ICP-MS) | < 0.6 ppm |
| Microbial screening | Pass (USP <2021>) |
| Certificate of Analysis | COA-VR-26-1147 |
Allergens and formulation
Vigor Rise is non-GMO and free from added artificial colors. As with any supplement made in a shared facility, traces of common allergens cannot be fully excluded, so if you have a serious allergy, review the label and check with your provider first.
See the live results for your bottle on the verification page, or read the full ingredient panel.