— Eight integrated services

Formulation, regulatory compliance and product development built as one.

From ingredient selection through stability testing, documentation, and manufacturing handover — every step built around EU requirements for your product category.

Overhead close-up on a laboratory bench: a glass beaker of white cream emulsion beside a small pipette, controlled studio lighting, clean white surface, no people
Overhead close-up on a laboratory bench: a glass beaker of white cream emulsion beside a small pipette, controlled studio lighting, clean white surface, no people
Flat-lay overhead of capsules, tablets, and powder in small glass containers on a white lab bench, bright overhead studio lighting, precise arrangement
Flat-lay overhead of capsules, tablets, and powder in small glass containers on a white lab bench, bright overhead studio lighting, precise arrangement
Close-up overhead of vape device components and liquid vials arranged on a clean white surface under controlled studio lighting, no people
Close-up overhead of vape device components and liquid vials arranged on a clean white surface under controlled studio lighting, no people
Stability test chamber interior with rows of labelled product vials on metal shelves, cool fluorescent lighting, clean and ordered laboratory environment
Stability test chamber interior with rows of labelled product vials on metal shelves, cool fluorescent lighting, clean and ordered laboratory environment
/ What we cover

Category-specific. Compliance-first.

Cosmetic Formulation & R&D

Food Supplement Development

Vape Product Development & EU-CEG

Stability & Compatibility Testing

Emulsions, serums, and active formulations developed against EU Cosmetics Regulation 1223/2009. PIF-ready ingredient selection from day one.

Nutraceutical formulation, dossier preparation, and notification-ready documentation built around EU food supplement directives.

Accelerated and real-time stability protocols, ingredient compatibility screening, and test data structured for regulatory submission.

Electronic vaping product development for the European market with full EU-CEG notification preparation and TPD compliance support.

Regulatory Documentation & PIF

Labeling Compliance

Manufacturing Handover

Product Positioning & Launch Support

Full Product Information File assembly for CPNP submission, cosmetic safety assessment coordination, and structured technical dossiers for all product categories.

Label text, mandatory declarations, and claims reviewed against EU category-specific requirements before artwork is finalized — not after.

Scale-up guidance, batch documentation, and manufacturer briefing packages that transfer your validated formula without compliance gaps.

Category positioning, claim substantiation, and market-entry documentation aligned with your target EU market and distribution channel.

Overhead flat-lay on a lit desk: printed regulatory documents and a Product Information File binder open to a technical page, a pen resting beside it, north-facing daylight, precise and orderly
Overhead flat-lay on a lit desk: printed regulatory documents and a Product Information File binder open to a technical page, a pen resting beside it, north-facing daylight, precise and orderly
▸ EU compliance built in

No compliance gaps at handoff.

Regulatory blockers surface in manufacturing when no one caught them at formulation. Every service here is connected — ingredient decisions, stability data, and label claims are cross-checked from the first technical brief.

PIF, CPNP, food supplement dossiers, EU-CEG: the documentation your product needs is structured throughout the engagement, not assembled at the end.

Ready to assess your product?

Tell us your category and where you are in development. We will identify which services apply and what your EU compliance path looks like.