FDA facility registration
Confirm that manufacturing, packing, and holding facilities have the registration status the US entry record expects.
21 CFR 1.225 · FD&C Act §415Nurbell connects each product profile and route to the obligations that can stop cargo, then turns the result into a clear shipment-readiness plan with every finding tied to a source.
Food cargo is often stopped by an obligation that is easy to miss upstream: an animal-origin permit, a residue threshold, an entry filing, or a licence tied to the importer. Nurbell brings those checks into the shipment workflow before booking.
Confirm that manufacturing, packing, and holding facilities have the registration status the US entry record expects.
21 CFR 1.225 · FD&C Act §415Surface the filing owner and timing obligation before the shipment reaches the carrier or border.
21 CFR 1.279 · Part 1 Subpart IIdentify animal-derived products that need an importer-led admissibility and permit review before departure.
9 CFR 94 · 9 CFR 95Bring destination residue limits, origin-specific controls, and supporting laboratory evidence into one readiness view.
Reg (EC) 396/2005 · (EU) 2019/1793Flag allergen and destination-language requirements before artwork and commercial documents are locked.
FALCPA · 21 CFR 101 · EU FICCheck the importer licence, market notification, and health-certificate path that applies to the lane.
SFCR · Japan Food Sanitation Act · CFIA AIRSElectronics blockers cluster around conformity, restricted substances, producer responsibility, and battery transport. Nurbell maps product attributes and route details to the evidence a carrier, importer, or market authority will ask for.
Identify emissions, immunity, and radio-equipment obligations from the product profile and destination.
47 CFR Part 15 · 2014/30/EU · 2014/53/EUConfirm the declaration, technical evidence, and applicable legislation before the product is placed on the EU market.
CE marking · EU Declaration of ConformitySurface substance restrictions and declaration evidence that must travel with the product compliance file.
2011/65/EU · REACH 1907/2006Flag the test summary and transport-document path before a carrier rejects battery-powered cargo.
UN Manual of Tests and Criteria, subsection 38.3Identify producer-responsibility, registration, and marking obligations before commercial launch.
(EU) 2023/1542 · 2012/19/EUCheck whether an energy-related product needs a label, product information, or supporting registration.
(EU) 2017/1369You can still run a pre-check. Listed categories have additional product-specific obligations mapped into the workflow.
Yes. A category is labelled live only when its rules, sources, review record, manifest entry, and regression tests ship together.
Official sources are collected and reviewed before changes reach customer-facing pre-checks. Current API coverage reports 6 live markets.