Registration process
Belgium vape product registration
Belgium follows the standard EU Tobacco Products Directive (2014/40/EU) notification process, but includes a regulated submission fee, a review process, and post-payment data verification by authorities.
Step 1: Prepare the Submission Data
Using TPD PRO, compile all required product information into an EU-CEG - compliant XML structure:
Submitter and Manufacturer details
Ingredient-level Composition with toxicological data
Presentations (market-specific formats)
Emission tests, packaging, leaflet, and other required files
Step 2: Submit via eTrustEx
Log in to eTrustEx and submit the following files in order:
Submitter XML (submitted once per Submitter ID)
Attachments (PDF files: emissions, tox, packaging, leaflet, etc.)
Submission XML (for each product)
Wait for Success confirmation after each stage.
Step 3: Government Fee and Invoicing
During the 6-month notification period, the Belgian inspectorate will issue an official invoice for the submission.
Fee: €250 per product
Payment is required for product evaluation and listing
Monitor your provided contact email for invoicing notifications
Step 4: Post-Payment Review
After payment, the inspectorate will:
Review the full submission contents
If any issues are found in one or more products, a notification will be sent with a request to correct the data
After corrections are submitted, all products in the batch will be reviewed again
⚠️ Ensure your initial submission is accurate to avoid delays and repeated review cycles.
Step 5: 6-Month Notification Period
As required by EU regulations, products can only be placed on the Belgian market 6 months after submission.
Step 6: Public Listing
Once all reviews are completed and approvals granted, your products will be published on Belgium’s official health authority website:
This site provides public access to the list of legally notified e-cigarette and nicotine products.
Summary
To successfully notify products in Belgium:
Prepare and submit via TPD PRO + eTrustEx
Pay €250 per product upon invoicing
Respond to any correction requests promptly
Wait 6 months for legal placement on the market
Final listing will appear on the government health portal