Selective by design.
A scoped process, direct to the chemists.
Selective by design. We cap our engagements to ensure every brand gets the focus required for prestige execution.
- FDA-Registered (Drug & Cosmetic)
- cGMP-Compliant
- ISO 22716 Certified
- MoCRA Registered
- Formulating Since 1997
Our standard MOQ for custom formulation ensures manufacturing efficiency.
From brief approval to the first physical iteration on your desk.
We limit concurrent large-scale custom developments to maintain speed.
The Engagement Process
- STAGE 01
The Scoped Consult
We review your brief, claims, target cost-of-goods, and timelines. If it's a fit, we provide a clear proposal for development.
- STAGE 02
Development & Iteration
Flat development fee (credited toward your first production order). We iterate until the texture, performance, and stability meet the standard.
- STAGE 03
Testing & Substantiation
Stability and FTIR raw-material testing run in-house. Everything else — preservative efficacy (PET), package compatibility, analytical work, and clinical claim testing — runs through independent third-party labs (billed at cost).
- STAGE 04
Production
Manufactured, filled, and assembled in our Moonachie, NJ facility. We cap the number of partners we take on so prestige work gets the focus it needs.