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TPD Compliance Services

Thanks to the cooperation with institutional bodies and major industry participants, FEM2- Ambiente offers its customer a complete service to meet the obligations imposed by the Directive 2014/40 / EU, better known as TPD (Tobacco Products Directive).

FEM2- Ambiente is the ideal partner as it provides lab services carried out by skilled experts and using advanced instruments in cooperation with private laboratories, providing a superior service at competitive prices; cooperating with the competent regulative authorities (both at national and union level), FEM2-Ambiente can also supply its customers with consultant services in every aspects dealing with regulation and compliance to ensure that every products will meet the standards required by every Member State. FEM2-Ambiente collects all the data and will submit a notification (as Enterer) on behalf of the customer through the Common Entry Gate.

What we do to let a product become TPD-II 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.