Which countries and regulations does Aeroz cover?

The US (DSCSA §582), the EU (Digital Product Passport / ESPR, Battery Regulation, FMD, EUDR, and the Forced Labour Regulation), the UK, and the UAE / GCC (Tatmeen). One unit-level authentication layer is mapped to each market's regime.

What if my market or regulation isn't listed?

We map your regulation in the same fixed-fee, 14-day audit framework. The verification layer is regulation-agnostic, so a new market is a mapping exercise on top of the same unit-level identity and custody record.

What standards does Aeroz build on?

Open, interoperable standards: GS1 Digital Link for resolvable product identity, EPCIS 2.0 for the append-only custody event log, and ISO 22385 for the trust framework. This keeps the layer portable across markets and serialization platforms.

Do you support cross-border custody?

Yes. A single unit carries one cryptographic identity and one append-only EPCIS 2.0 custody log as it crosses borders, so the same record satisfies the rules of every market it moves through — no per-country re-tagging.

What is the FDA NDC-12 rule and when does it take effect?

The FDA's final rule (March 2026) moves every US drug product to a uniform 12-digit National Drug Code in a 6-4-2 format, effective 2033, carried in a GS1 2D data carrier such as DataMatrix. Every drug label in the US must be re-issued. Aeroz encodes NDC-12 in GS1 DataMatrix with AI(715) today, and pairs the barcode with a cryptographic chip so the new label is verifiable — not just readable.

What is the UN Transparency Protocol (UNTP) and does Aeroz support it?

UNTP is a UN/CEFACT framework for interoperable digital product passports and verifiable supply-chain credentials that any country can consume. Aeroz issues UNTP-conformant digital passports signed against the unit's chip identity, so one record works across jurisdictions.

Which compliance deadlines are coming first?

DSCSA §582 unit-level requirements are enforced from Nov 27, 2026 in the US. The EU Battery Passport (Art. 77) applies from Feb 18, 2027. EU Digital Product Passports phase in by sector 2027–2030 under ESPR. The EU Forced Labour Regulation applies from late 2027, and the FDA's NDC-12 labeling rule takes effect in 2033.

Global Compliance · DSCSA, EU DPP, FMD & Tatmeen

How global works

Authenticate once. Comply everywhere.

A product crosses borders; its regulation changes at each one. Aeroz binds a single cryptographic identity to the unit, then exports the proof in the format each jurisdiction expects — no second tag, no parallel system per country.

One chip identityGS1 Digital LinkEPCIS 2.0 eventsPer-market export

How the chip works →

Markets mappedUS · EU · UK · GCC

Identity per unitAES-128

Verification scan<300ms

Recall traceback<60s

New-market audit14 days

Region by region

Each market. Its own rulebook.

The regulation that applies, when it bites, what it requires, and the role Aeroz plays — by region.

United States

DSCSA · unit-level security

DSCSA §582 (21 U.S.C. § 360eee-1) · enforced Nov 27, 2026 · FDA Form 3911

RequiresEnhanced unit-level traceability, verification, and recall response

Aeroz roleUnit authentication, saleable-returns checks, sub-60s traceback

European Union

EU DPP, Battery, FMD, EUDR

ESPR 2024/1781 · Battery Reg. 2023/1542 Art. 77 · FMD 2011/62/EU · EUDR 2023/1115 · Forced Labour Reg. 2024/3015

RequiresData carrier, Digital Product Passport, due-diligence and provenance records

Aeroz roleDurable physical carrier for the DPP and its custody record

United Kingdom

Post-Brexit divergence

FMD divergence (post-Brexit) · UKCA marking · DEFRA deforestation rules

RequiresUK-specific conformity marking and a separate deforestation due-diligence track

Aeroz roleOne identity exported to both EU and UK formats, no re-tagging

UAE · GCC

Tatmeen & Made-in-UAE

Tatmeen track-and-trace · Made-in-UAE · DMCC free-zone trade

RequiresSerialized aggregation reporting and verifiable origin of goods

Aeroz roleConfirms the physical pack matches the Tatmeen record; proves origin

United States · Pharma labeling

FDA NDC-12 & the GS1 2D transition

FDA final rule (Mar 2026) · 12-digit 6-4-2 NDC · effective 2033 · GS1 DataMatrix

RequiresEvery drug label re-issued with the uniform 12-digit NDC in a 2D data carrier

Aeroz roleEncodes NDC-12 in GS1 DataMatrix + AI(715) today — and pairs it with the chip so the label itself is verifiable

Global · UN framework

UN Transparency Protocol (UNTP)

UN/CEFACT · digital product passports & verifiable credentials · cross-border

RequiresInteroperable, verifiable supply-chain credentials any country can consume

Aeroz roleIssues UNTP-conformant digital passports signed against the unit's chip identity — one record, every jurisdiction

The clock

Every mandate has a date.

When each regime starts to bite — and what has to be true at the unit level by then.

Live nowFMD · Tatmeen · DFARSSerialization & custody already enforced

Nov 27, 2026DSCSA §582Unit-level verification, US pharma

Feb 18, 2027EU Battery Art. 77Passport on every in-scope battery

Late 2027Forced Labour Reg.Auditable origin evidence

2027–2030EU DPP · ESPRPassports phased in by sector

2033FDA NDC-12Every US drug label re-issued in GS1 2D

Deadline	Regime	What must be true	How Aeroz gets you there
Nov 27, 2026	DSCSA §582 (US)	Unit-level verification, enhanced tracing, and recall response across the pharma chain	Chip-verified units, saleable-returns checks, <60s Form 3911-ready traceback
Feb 18, 2027	EU Battery Reg. Art. 77	A battery passport on every LMT, industrial >2 kWh, and EV battery placed on the EU market	Durable dual-frequency carrier + passport record bound to the physical pack
2027–2030	EU DPP · ESPR	Digital Product Passports phased in sector by sector, on a data carrier that survives the product's life	Chip + GS1 Digital Link as the tamper-proof physical anchor for each passport
Phasing in	EUDR	Geolocated, deforestation-free provenance and due-diligence statements for in-scope commodities	Plot-level provenance bound to the unit; due-diligence statement export
Late 2027	EU Forced Labour Reg.	Demonstrable, auditable knowledge of where and how goods were made	An append-only custody record from origin — evidence, not attestation
2033	FDA NDC-12	All US drug labels re-issued with the 12-digit NDC in a GS1 2D data carrier	NDC-12 in DataMatrix + AI(715) now; chip pairing makes the new label verifiable, not just readable
Live now	FMD (EU/UK) · Tatmeen (UAE) · DFARS (US)	Serialization, decommissioning, aggregation reporting, counterfeit-electronics custody	One identity mapped to each regime's reporting format — no parallel systems

Standards & interoperability

A seat at the table on the global DPP standard

Aeroz is a member of INCITS and participates in the U.S. Technical Advisory Group to ISO/IEC JTC 5 — Digital Product Passport, the international committee developing cross-system interoperability standards for DPPs. We build to where the standard is going.

Membership in the standards process; not an endorsement or certification of Aeroz or its products by INCITS, ANSI, or ISO/IEC.

Our DPP solution →

Built on open standards

The same standards regulators reference.

Aeroz speaks the interoperable standards every regime above is converging on — so the proof reads the same in Washington, Brussels, London, and Dubai.

Resolution

GS1 Digital Link

One scannable identifier resolves to the data each market needs, from one URL on the unit.

Event model

EPCIS 2.0

Every custody change — commission, ship, receive, dispense — as a standardized, exportable event.

Identifier scheme

ISO 22385

An interoperable framework for trust and authentication that travels across jurisdictions.

Framework14-day audit

OutputWritten map

EngagementFixed fee

CommitmentNone

Selling somewhere else?

A market we haven't listed?

New mandates land every quarter, and yours may not be above yet. We map your regulation in the same 14-day audit framework — a written gap analysis, the standards that apply, and a scoped path to compliant.

Map my regulation →

Global compliance audit

Map every market — in 14 days.

A fixed-fee Aeroz audit produces a written gap analysis against each regime you sell into, an EPCIS-readiness assessment of your stack, and a scoped remediation plan with cost and timeline.

Turnaround

14 days

Engagement

Fixed fee

Deliverable

Written report

Commitment

None to proceed

Start a global audit → A market not listed →

Fixed fee 14-day written report No commitment to proceed

What's included

Per-market gap analysis against DSCSA, EU DPP, FMD, EUDR, Tatmeen.
Standards readiness — GS1 Digital Link, EPCIS 2.0, ISO 22385.
EPCIS 2.0 assessment across TraceLink, Antares, MediLedger.
Recall-traceback simulation to time-baseline your response.
Pilot scope for one SKU or line, mapped to every market.