Manufacturing Benchmarks & Quality Testing for Olivaro
Our stringent analytical testing protocols, cGMP cleanroom manufacturing standards, and heavy metal screening procedures.
All units of Olivaro are formulated exclusively within an FDA-registered manufacturing facility situated in the United States, operating under current Good Manufacturing Practices (cGMP 21 CFR Part 111) and certified by third-party auditors.
The 4 Pillars of Product Testing
1. Identity Verification
Raw botanical extracts undergo High-Performance Thin-Layer Chromatography (HPTLC) to verify species identity and active marker concentrations.
2. Heavy Metal ICP-MS
Inductively Coupled Plasma Mass Spectrometry verifies that lead, arsenic, cadmium, and mercury levels remain well below strict USP thresholds.
3. Microbial Assays
Screened for aerobic plate count, yeast, mold, E. coli, and Salmonella prior to release from quarantine.
4. Temperature Controlled Storage
Finished bottles are stored in a climate-controlled warehouse held between 65°F and 72°F to preserve phytochemical stability.
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Olivaro Official Supply