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Compliance and Regulatory

Each EU Member State is required to implement this Directive in order to adopt rules, terms and penalties related to the production, distribution and communication of electronic cigarettes and e-liquid containing nicotine.



The compliance service offered by FEM2-Ambiente aims to assess that the products comply the norms fixed by every single Member States where the manufacturer or importer intends to market its product.

FEM2-Ambiente will evaluate every aspects subjected to regulation in order to fulfill the obligations set out by local transposition of the Directive. Whereas the product is compliant, a full documentation will be released together with the manufacturer/importer in order to demonstrate compliance. Otherwise, a customized R&D service will be offered to accordingly modify the product and make it compliant, without changing its desired features.

Once issued the documentation, a notification service is supplied: FEM2-Ambiente will submit a notification of behalf of the manufacturer/importer, allowing him to obtain the EC-ID code needed to market the product in the European Union.

What we do to let a product become TPD2 compliant

in brief

1
GETTING TO KNOW YOUR COMPANY PROFILE AND PRODUCTS:

fulfillment of the dedicated form . Of course after having sign an NDA: you can trust us, but we want to be sure you’ll be. After that, you will receive our quote.

2
SUBMISSION OF SAMPLES TO BE ANALYZED AND PROFILING OF YOUR COMPANY IN THE EU-CEG PORTAL:

we will check that everything’s ok and then we will move forewords; we will get a Submitter ID on behalf of you.

3
TOXICOLOGICAL LITERATURE SEARCH

and issuing of a complete risk assessment report concerning every relevant ingredient of the blend. After that we will set up a testing solution suitable for your needs.

4
ANALYSIS OF THE EMISSIONS

and issuing of an analytical report. Parameters and conditions will be set as function of the type of products and markets.

5
COMPLIANCE

we will check every details to guarantee your product is compliant. If not, we will evaluate together how to proceed to obtain compliance.

6
PRODUCTION OF TECHNICAL DOSSIER.

through the integrated evaluation of information from manufacturer, analytical labs and from toxicological risk assessment.

7
SUBMISSION OF NOTIFICATION.

You will receive the EC-ID and you will be then ready to market your products in the European Union.