Our standard
AncientModern.ai’s product promise depends on sourcing and testing. If users can grow or make at home, we need to explain when our version is better: identity verification, contamination testing, standardized extracts, batch consistency, and documented suppliers.
Raw material qualification
- Botanical identity verified by supplier documentation and appropriate testing.
- Country of origin and processing site documented.
- Lot-specific Certificate of Analysis.
- Heavy metal review, especially for roots, minerals, and imported botanicals.
- Microbiological testing for powders and tea materials.
- Pesticide and residual solvent review when applicable.
- Adulterant screening for high-risk botanicals.
Finished product testing
Finished products should be tested for identity markers where feasible, heavy metals, microbial contamination, and label-relevant standardization markers. Extract-heavy capsules require particular care.
Manufacturing
Dietary supplement manufacturing in the U.S. is subject to 21 CFR Part 111 cGMP requirements for those who manufacture, package, label, or hold supplements. Our manufacturer RFP requires cGMP compliance, quality documentation, and batch records.