Export to Europe · Diagnostic

Score your Europe export readiness.

Against the six realities a producer has to clear to supply the European medical market. Six questions, a few minutes. Answer honestly; the point is to find out where you are export-ready and where Europe's gate will stop you.

Reality 01 · EU-GMP records

Are your manufacturing, packaging, and test records EU-GMP-grade, immutable, and inspection-ready as a byproduct of operating?

Reality 02 · Traceability

Does every production and test record carry the lot and batch identifier, so GACP-to-GMP continuity is the ledger?

Reality 03 · QP release

Can you assemble a complete, consistent documentation dossier for a European Qualified Person to release a batch, from one source?

Reality 04 · Permits

Do your import-permit and shipment dossiers draw their batch numbers and quantities directly from the batch record, not re-keyed?

Reality 05 · B2B export commerce

Do you manage European importers as documentation-bound B2B wholesale accounts, with batch records and CoAs attached, on one ledger?

Reality 06 · ERP integration

Do your financials, inventory, and export records run from one ledger, or do you reconcile a separate ERP against a separate system?

This diagnostic is a self-assessment, not legal advice or a formal compliance audit. It reflects where your commerce and records stack sits against Europe's import requirements, not whether your facility holds EU-GMP or your shipment meets every destination-country rule. For a formal review, talk to your counsel, your EU-GMP consultant and destination-country authorities, and the team at SellStack.