(E-cigarettes, Nicotine Pouches, Refill Containers, E-cigarette PODs, Devices Without E-Liquid)
Step-by-Step Guide for Manufacturers and Importers
To comply with the Tobacco Products Directive (2014/40/EU), all manufacturers and importers must notify their products via the EU Common Entry Gate (EU-CEG) before placing them on the EU market.
This includes:
E-cigarettes (with or without liquid)
Refill containers (including PODs)
Nicotine pouches
Other tobacco or nicotine substitute products
❗ You must notify your product at least 6 months before its planned market launch.
🔐 Registering a Submitter ID
Before you can submit anything, you need to obtain a Submitter ID — a unique 5-digit number used to identify your company in the EU-CEG system.
🔽 Step-by-Step Registration
Create an EU Login Account:
https://ecas.ec.europa.eu/cas/loginDownload the Submitter ID Form (PDF):
Submitter ID Form (Official Download)
(Open in Adobe Acrobat Reader to complete the form properly.)Fill in the form and attach required documents, such as:
Company registration certificate
Utility bill or tax number (as proof of operation)
Send the completed form to:
SANTE-SUBID-EUCEG@ec.europa.eu
📌 Processing may take several days. Once approved, you will receive your Submitter ID. Later, a Party ID will be issued — required for submitting XML data.
📂 What Product Information Must Be Submitted?
Each product submission must include:
✅ Product design and classification
✅ Product name, brand, and target market country
✅ Ingredient list with toxicological data
✅ Emission test results (if applicable)
✅ Conformity assessment (if applicable)
✅ Description of production process
✅ Packaging images & instruction leaflet (required in some Member States)
💻 How to Submit Your Product
Option A: Manual Process (EU XML Creator Tool)
Download XML Creator Tool: EU XML Creator (CIRCABC Library)
Fill in:
Product title, CLP classification
Substance & ingredient data
Emission values and toxicology details
Use built-in validation tool
Export your XML file
Log in to the eTrustEx platform:
https://euceg.ec.europa.eu/etrustex/inbox.doUpload your XML file and submit
If successful, the 6-month waiting period will begin — your product is now officially under EU-CEG review.
Option B: Use TPD PRO Platform (Recommended)
Avoid time-consuming manual steps. TPD PRO is an advanced EU-CEG submission platform that automates the entire process:
✅ Smart forms instead of XML complexity
✅ Built-in toxicological templates
✅ Automatic formatting & validation
✅ Ready-to-export XML in seconds
✅ Multiple language support
✅ Package preview uploads
✅ Historical logs for audits and re-submissions
TPD PRO is faster, easier, and fully aligned with EU-CEG requirements — trusted by professionals for accuracy and speed.