Three-Tier Analytical Quality Standard
How every bottle of Maxorin is manufactured, audited, and tested under Title 21 CFR Part 111 cGMP regulations and USP standards.
Botanical Raw Testing
Incoming raw herbs and amino acids are quarantined immediately upon delivery. Identity is validated via Fourier-Transform Infrared (FTIR) spectroscopy to guarantee authentic botanical species prior to blending.
Cleanroom Encapsulation
Manufacturing takes place inside HEPA-filtered cleanrooms in Aurora/Denver, CO. Environmental temperature, humidity, and fill weights are logged every 15 minutes to guarantee exact uniform potency per capsule.
Third-Party Laboratory Assays
Representative samples from each finished lot are sent to independent ISO-17025 accredited testing laboratories to verify HPLC active potency and clear USP 2232 heavy metal screening thresholds.
USP 2232 Heavy Metal Safety Thresholds
| Contaminant Tested | USP 2232 Threshold | Maxorin Batch #2026-M84 Result | Status |
|---|---|---|---|
| Lead (Pb) | < 0.50 ppm | < 0.01 ppm | PASS |
| Arsenic (As) | < 1.50 ppm | < 0.02 ppm | PASS |
| Cadmium (Cd) | < 0.50 ppm | < 0.01 ppm | PASS |
| Mercury (Hg) | < 1.50 ppm | < 0.005 ppm | PASS |