Formulation, regulatory compliance and product development built as one.
One continuous engagement from feasibility to manufacturing handover. No vendor gaps, no compliance surprises at submission.
Feasibility & Ingredient Selection
We assess technical and regulatory feasibility before a single gram is weighed. Ingredient lists are screened against EU cosmetic, supplement, and vape regulations from day one.
Prototype Development
Bench-scale prototypes are developed iteratively against defined performance criteria. Each iteration is documented; nothing advances without a traceable record.
Stability Testing & Full Documentation
Stability and compatibility protocols run in parallel with documentation — PIF compilation, safety assessments, and labeling compliance are built as the formula matures, not after.
Manufacturing Handover
Clients receive a complete, audited dossier ready for submission. The manufacturing partner gets a specification pack with no gaps to fill and no rework to commission.
Regulatory checkpoints at every phase
EU Cosmetics Regulation, food supplement directives, and EU-CEG vape requirements are checked at each decision point — not reviewed once formulation is locked. This is what eliminates late-stage blockers.
Ready to start your development sequence?
Tell us your category and where you are in development. We map the technical and regulatory path from there.