Documentation built into the development process.
Cosmetics, food supplements, vape. Three distinct regulatory frameworks — one structured engagement. Dossiers, PIF files, and EU-CEG notifications prepared from formulation forward.
EU compliance across every category we serve.
Cosmetics — PIF & CPNP
Food Supplements — EFSA Dossier
Vape — EU-CEG & TPD
Full Product Information File preparation under EU Cosmetics Regulation 1223/2009. Safety assessment coordination, CPNP notification, and labeling compliance reviewed at formulation stage.
Dossier preparation following EFSA guidelines and national competent authority requirements across EU member states. Ingredient substantiation and claim documentation included.
EU-CEG notification preparation and EU TPD compliance integrated into the vape development sequence. Regulatory blockers identified at ingredient selection, not at submission.
The dossier is not a final step.
Every ingredient decision, stability protocol, and compatibility assessment feeds directly into the regulatory file. Documentation is structured from day one — not reconstructed from lab notes at the end.
This means your PIF, supplement dossier, or EU-CEG notification reflects the actual formulation — tested, traceable, and ready for competent authority review.
Bring your regulatory question to us first.
Whether you are preparing a first PIF, structuring a supplement dossier, or navigating EU-CEG requirements, a direct consultation with our team is the fastest way to scope the work accurately.