Regulatory assessment
EU Import Compliance Assessment
Know what needs checking before you commit to an EU import.
Sourcing, shipment, import and market placement involve different decisions. This assessment considers your product configuration, supply chain and proposed import setup together, identifying regulatory evidence and unresolved questions at the relevant stage.
Identify regulatory requirements, documentation gaps and critical steps before sourcing, shipping and importing products into the EU.
€249.00 incl. VAT
One assessment case · 180 calendar days of active editing access from purchase · two substantive report snapshots, each as a German and an English PDF.
Your practical benefits
Prepare early decisions: Identify unresolved requirements before ordering and shipment.
Clarify responsibilities: Consider manufacturer, importer and own-brand arrangements.
Make focused supplier requests: Structure the evidence and follow-up actions needed.
Turn an import plan into a practical review agenda
Discovering missing evidence after shipment makes planning harder. The case-specific assessment connects product and operator facts with supported regulatory routes and the relevant sourcing and import stages. Unknown facts and matters requiring external review remain explicit.
What you receive
A structured import-compliance report describing the product and supply-chain setup, stage-specific review points, evidence gaps and prioritised actions for the next decisions.
Two substantive report snapshots are provided for one case, each with a German and an English PDF. Retrieving an existing PDF does not create a new report snapshot.
How it works
- Describe the product, target markets and proposed sourcing and import setup.
- Record operator roles, supplier evidence and the current sourcing or shipment stage.
- Address open points and plan the next actions before ordering, shipment or market placement.
Who it is for
Importers, procurement and sourcing teams, own-brand businesses, non-EU manufacturers and product compliance teams.
Good to know
The assessment supports regulatory decisions within the supported routes. It does not execute imports or replace customs classification, tax advice, laboratory testing, certification or regulatory approval.
The 180-day period covers active case editing and creating the included report snapshots. It does not promise continuous legal monitoring or determine data-deletion periods. The agreed retrieval entitlement applies to stored reports.
Frequently asked questions
Must I complete the free market check first?
No. You can go directly to the import assessment if you already know your question.
Is available documentation automatically accepted as sufficient?
No. Available, missing and unresolved evidence are considered separately.
Can I continue after a supplier responds?
During the 180-day period you can work on the case and create a second substantive report snapshot within the agreed scope.
Related decision perspectives
Optional: free EU Market Check for a product
EU Market Access Assessment
Identify applicable EU product regulations, required compliance evidence and the next steps to bring your product to the EU market.
Product Release Readiness Assessment
Determine your product's regulatory release readiness, identify missing evidence and prioritize the actions needed before market launch.