Knowledge base

Docs & guides

Everything we know about TPD, EU‑CEG, MHRA and the rest of the alphabet soup — explained without the jargon.

Getting started

  • What is TPD?
    The Tobacco Products Directive in 5 minutes.
  • What is EU‑CEG?
    The submission system used by all 27 member states.
  • Do I need to register?
    Decision tree for vape products entering the EU.

By market

  • EU member states
    Country‑specific quirks: Germany, France, Italy, Spain…
  • United Kingdom (MHRA)
    Post‑Brexit notifications and what changed.
  • Translations & languages
    Which markets require local language SDS.

Lab testing

  • Required test panels
    Chemical composition, emissions, heavy metals.
  • Choosing an accredited lab
    What ISO 17025 actually means.
  • Reusing test data
    When a test for one SKU covers others.

SDS & safety

  • Writing a compliant SDS
    Section by section, GHS/CLP rules.
  • When to update an SDS
    Triggers that require a new version.

Packaging

  • Warning text & pictograms
    Sizes, fonts, placement.
  • Leaflet requirements
    What must be inside the box.
  • Unique identifiers (UI)
    Track & trace codes for tobacco‑adjacent products.

FAQ

  • How long does TPD take?
    Realistic timelines per market.
  • What does it cost?
    Per‑SKU and per‑market pricing factors.
  • Can you help with rejected submissions?
    Yes — turnaround is usually under a week.

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