Phase 01 — Discovery & R&D
Our scientists work with you to define efficacy benchmarks, bioavailability requirements, and ingredient synergies.
- Ingredient sourcing network access
- Stability prediction modeling
A transparent, stage-gate process from concept to commercial scale.
Our scientists work with you to define efficacy benchmarks, bioavailability requirements, and ingredient synergies.
Small-scale production runs to verify texture, flavor profile, and active integrity.
Rigorous internal and third-party laboratory analysis for purity and potency.
Full-scale manufacturing in our temperature-controlled facility with automated high-speed packaging lines.
Direct-to-warehouse shipping with full cold-chain support and regulatory documentation.
Our facility is optimized for multiple delivery formats, ensuring your custom formulation reaches its maximum potential.
| Technical Specification | Our Standard |
|---|---|
| Minimum Order Quantity | Low MOQs available for pilot programs |
| Active Ingredient Testing | HPLC, ICP-MS, Micro-biological analysis |
| Regulatory Support | Label review, COA issuance, FDA compliance |
| Flavor Systems | Natural, non-GMO, organic options |