EU Buyers Guide

This guide is written for EU buyers who want fewer surprises: fewer paperwork failures, fewer disputes, and fewer “it should be fine” moments.
It is conservative by design. It is not legal advice, and it does not promise clearance, delivery timelines, or outcomes.
Your advantage is discipline: documentation, verification, and traceability.

Core hubs: Wholesale · Documentation ·
Compliance · Shipping ·
Legal status · Insights


Who this guide is for

  • B2B buyers sourcing wholesale who need audit-ready batch files
  • Teams with internal approvals (ops, compliance, finance) who need repeatable checklists
  • Buyers shipping cross-border who want a realistic risk posture

Who this guide is NOT for

  • Anyone looking for “guaranteed legality” or “guaranteed delivery” language
  • Buyers who don’t want to verify labs or maintain records
  • Teams that want to improvise policies mid-dispute

The EU buyer mindset: stop buying on assumptions

EU procurement is rarely forgiving of sloppy documentation. Your job is not to “win debates” about edge cases.
Your job is to maintain a controlled batch file and make decisions you can defend internally.

Rule: If you can’t explain the batch with a coherent document set in under 3 minutes, you don’t have a professional batch file.


EU buyer workflow (documentation-first)

Step 1 — Define internal acceptance specs (before purchase)

  • Potency interpretation: how you treat THCA vs Δ9-THC and any “Total THC” line items (reference: THCA vs THC).
  • Contaminant expectations: panel categories you require (risk-based; enforce consistently).
  • Documentation completeness: minimum COA fields and batch linkage.
  • Retest/referee policy: what happens if results conflict and which lab governs.

Build your SOP using /documentation/quality-assurance/.

Step 2 — Validate the batch file (do not skip)

Step 3 — Build the shipment packet (before dispatch)

The shipment packet is what you send when a hold happens. If you can’t assemble it fast, you’re not ready.

  • Invoice + packing list + batch map
  • COA set for each batch/lot in the shipment
  • Lab verification note stored with the packet

Use /documentation/shipping-flow/ and
/compliance/shipping-documents/.

Step 4 — Receiving controls (protect yourself)

  • Photo log on arrival (outer carton, inner packaging, labels, seals, damage)
  • Label check: batch/lot ID matches the batch file
  • Quarantine triggers defined (mismatch, damage, broken seals)

Storage discipline matters: /compliance/storage-handling/.


Inspection risk posture (what serious buyers assume)

EU buyers should assume that inspections and holds can occur. Your job is not to predict them—it’s to be ready.

  • Do not promise outcomes to your own customers unless you control the risk.
  • Do not rely on “one COA file”—you need a coherent shipment packet.
  • Do not ship with identity ambiguity (batch IDs must match across everything).

Read: /insights/thca-customs-inspections/ and
/documentation/risk-disclosure/.


EU buyer checklists

Pre-order checklist

  • Destination country confirmed and internal policy aligned (context hub: /legal-status/).
  • Acceptance specs written (potency, contaminants, documentation completeness, packaging/labeling).
  • MOQ and pricing expectations understood (MOQs, pricing structure).

Pre-dispatch checklist

Receiving checklist

  • Photo log recorded immediately.
  • Labels match batch/lot IDs on paperwork.
  • Damaged or mismatched goods quarantined per SOP.

Where this guide connects inside the site


FAQ

Is this guide legal advice for operating in the EU?

No. This is operational guidance for documentation and procurement discipline. For context references, use /legal-status/
and consult qualified professionals for decisions.

Do you guarantee customs clearance or delivery?

No. See /shipping/ and /documentation/risk-disclosure/.

What’s the fastest way to reduce EU procurement risk?

Enforce batch traceability and decision-grade COAs: /compliance/batch-traceability/ and
/compliance/certificate-of-analysis/.

Where do I standardize COA review?

Use /documentation/sample-coa/ as the field checklist and enforce requirements via
/compliance/certificate-of-analysis/.

What should we do if a shipment is held?

Respond with a coherent shipment packet (invoice + packing list + batch map + COAs + verification note), and document the event internally.
Reference: /documentation/shipping-flow/ and
/insights/thca-customs-inspections/.