20 May 2016TPD-II comes in force. For new products which companies intend to put on the market between 20 May to 19 November 2016, the application must be made on 20 May 2016.
Important:from 20 May 2016 onwards, producers/importers of new e-cigarettes and refill container products will need to submit a notification 6 months before putting their product on the market. A product which has been substantially modified will count as a new product and must also follow this process. Further information regarding what qualifies as a substantial modification will be made available.
20 November 2016:Producers of all e-cigarettes and refill containers that are covered by the TPD and are on the market before 20 May 2016 will have until 20 November 2016 to submit a notification.
Important:until 20 May 2017 it will be possible to sell through stock of products that do not comply with the labelling and product composition requirements of the TPD. Batches of products which do not comply with these requirements may only be sold if they were produced before 20 November 2016.
What we do to let a product become TPD2 compliant
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.
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.
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.
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.
we will check every details to guarantee your product is compliant. If not, we will evaluate together how to proceed to obtain compliance.
PRODUCTION OF TECHNICAL DOSSIER.
through the integrated evaluation of information from manufacturer, analytical labs and from toxicological risk assessment.
SUBMISSION OF NOTIFICATION.
You will receive the EC-ID and you will be then ready to market your products in the European Union.