Regulatory compliance (GPSR / FDA)
Why this matters for your business
Selling regulated products (cosmetics, supplements, electronics, toys, food) requires per-jurisdiction compliance — EU GPSR (General Product Safety Regulation), US FDA, CE marking, Health Canada, etc. Each requires specific information displayed on the PDP + accessible to authorities. Get it wrong: fines, marketplace removal, recall liability.
Most stores treat this as a manual headache — different teams manage different regions; product info gets out of sync; compliance gaps go undetected until inspection.
The platform handles this systematically. Capture compliance fields once per product; the platform routes per-region appropriately and surfaces them on PDPs + makes them accessible to authorities.
What this typically unlocks
| Outcome | Result |
|---|---|
| Per-region compliance display | automatic |
| Compliance-related listing rejections | near 0 |
| Time on compliance per product | −85% |
| Regulator audit readiness | always |
What you actually get
| Capability | Description |
|---|---|
| Field capture | Manufacturer, importer, safety data sheets, etc. |
| Per-jurisdiction routing | Show EU GPSR fields to EU customers; FDA to US |
| Document storage | PDFs (test results, certifications) attached |
| Schema versioning | Compliance schema evolves; catalog stays current |
| Audit log | Every compliance change logged |
| Pre-publish gate | Block publication of non-compliant SKUs |
Real merchant scenarios
Scenario A — EU GPSR rollout
Setup. Brand selling cosmetics in EU. New GPSR took effect; all SKUs needed updated compliance info.
Pre-platform: Manual update per SKU × 240 SKUs = ~80 hours.
With compliance: Bulk-update template applied across SKUs. Auto-displayed on EU PDPs. ~4 hours total.
Scenario B — FDA cosmetics labeling
Setup. US brand needed FDA-compliant ingredient + warning labeling on PDPs.
Setup: Compliance template per FDA category. Each SKU matched to template; required fields enforced.
Result: All 180 SKUs FDA-compliant. Audit-ready documentation per SKU.
Scenario C — Multi-jurisdiction simultaneously
Setup. Brand selling supplements across US + EU + AU. Each has different rules.
Setup: Per-jurisdiction templates. PDP shows the right fields based on visitor region.
Result: Single product, properly displayed per market. No per-region SKU duplication.
Plan tiers
| Capability | Free | Starter | Pro | Agency | Enterprise |
|---|---|---|---|---|---|
| EU GPSR compliance | — | — | ✓ | ✓ | ✓ |
| US FDA compliance | — | — | ✓ | ✓ | ✓ |
| CE marking | — | — | ✓ | ✓ | ✓ |
| Document storage | — | — | ✓ | ✓ | ✓ |
| Multi-jurisdiction routing | — | — | ✓ | ✓ | ✓ |
| Pre-publish gate | — | — | ✓ | ✓ | ✓ |
| Custom regulatory schemas | — | — | — | — | ✓ |