— Greece — EU Regulatory Markets

Formulation, regulatory compliance and product development built as one.

From ingredient selection to PIF submission — cosmetics, food supplements, and vape products developed under a single structured process. No compliance gaps at handoff.

Extreme close-up overhead of a laboratory flat-lay: a row of amber glass vials, white cream-filled petri dishes, and capsule tablets arranged in a tight grid on a white surface under bright studio overhead lighting, clinical and precise, no hands visible, pure product detail
Extreme close-up overhead of a laboratory flat-lay: a row of amber glass vials, white cream-filled petri dishes, and capsule tablets arranged in a tight grid on a white surface under bright studio overhead lighting, clinical and precise, no hands visible, pure product detail
/ Three Categories. One Process.

EU-ready from day one.

Cosmetic Formulation & R&D

Creams, serums, emulsions — stability-tested and documented to EU Cosmetics Regulation 1223/2009, PIF and CPNP-ready.

Food Supplement Development

Capsules, tablets, and powder formats developed with full dossier preparation and EU regulatory documentation from formulation forward.

Vape Product Development & EU-CEG

End-to-end development for the European vape market: formulation, compatibility testing, and EU-CEG notification preparation.

+ Integrated from Day One

A structured sequence, no gaps.

01
02
03
04
Concept & Feasibility
Prototype & Stability
Regulatory Documentation
Manufacturing Handover

Ingredient selection, regulatory screening, and technical feasibility assessed before a single prototype is made.

Formulation development, compatibility assessment, and stability testing under controlled conditions before scale-up.

PIF preparation, dossier compilation, labeling compliance review, and EU-CEG notification — built in, not bolted on.

Documented formula and full technical file transferred to manufacturing. One handoff, complete file, no requalification gaps.

Your concept. EU-compliant and market-ready.

Tell us your category and regulatory target. We assess technical feasibility and map the documentation path before you commit to manufacturing.