We source the best,
or we don't source at all.
Every ingredient in every Neosoma formulation is selected, verified, and tested against pharmaceutical-grade standards.
What an Neosoma ingredient must be.
Identity-verified
Every raw material is tested by HPLC, mass spectrometry, or appropriate orthogonal method on receipt. No exceptions.
Mechanistically justified
If we can't point to peer-reviewed evidence of mechanism, it doesn't go in.
Bioavailability-validated
Form matters as much as substance. We require evidence the molecule absorbs at clinically relevant doses.
Independently certified
Third-party heavy metal, microbiological, and contaminant testing on every batch.
Where we manufacture.
Neosoma works exclusively with cGMP-certified facilities across the EU and North America. Our contract manufacturing partners hold ISO 22000, NSF, and where applicable, GMP+ certification. We do not work with facilities we have not audited.
Who we work with.
We partner with ingredient suppliers and contract manufacturers who meet the following baseline:
- Full COA on every shipment
- Country of origin transparency
- Heavy metals testing per USP <232> / <233>
- Microbiological testing per USP <2021> / <2022>
- Verified non-irradiated, non-ETO sterilization where applicable
- Allergen and GMO disclosure
- Audit-ready documentation
Are you an ingredient innovator or contract manufacturer?
If you've developed a novel active, hold IP on a proprietary form, or operate a facility that meets our standard — we want to hear from you. Neosoma is actively evaluating partners for upcoming formulation work across all three pillars.