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Quality Assurance

Manufacturing Benchmarks & Quality Testing for Olivaro

Our stringent analytical testing protocols, cGMP cleanroom manufacturing standards, and heavy metal screening procedures.

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Manufacturing Standard

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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