← Regulatory compliance / PPWR Declaration Assistant
Role sheet · Priority deadline August 12, 2026
PPWR Declaration Assistant
A role dedicated to your PPWR (EU 2025/40) declaration: packaging specification audit, void ratio, restricted substances, EU register. Named human reviewer. Single call — 1-hour diagnosis, then a 4-week pilot priced after your priorities.
Par Damien Godard, founder of Taranis AI · August 14, 2026
Visual shared with the Regulatory compliance pillar.
The problem: a PPWR declaration is not a formality
The PPWR regulation (EU 2025/40) applies in full from August 12, 2026. Any company placing packaging on the European market — regardless of its size — must be able to produce, at any time, a declaration of conformity per packaging reference: composition, recyclability, void ratio, restricted substances (PFAS banned from August 12, 2026, BPA from July 20, 2026).
Without this file, the block is immediate: market withdrawal, product recall, national sanctions. The volume of data to maintain (specifications by SKU, supplier attestations, recycled content, lab testing) does not fit in a spreadsheet — and cannot be delegated to a generic tool that does not know your internal referential.
The dedicated assistant we deploy tackles this volume: packaging data collection from suppliers, verification against current PPWR requirements, timestamped audit trail, and systematic human review by your Quality Manager before any publication.
● IN scope
- ✓Audit of packaging specifications (materials, mass, volume, void ratio ≤ 40%).
- ✓Verification of restricted substances (PFAS from 08/12/2026, BPA from 07/20/2026).
- ✓Build and maintain the EU register per packaging reference.
- ✓Generation of the declaration of conformity and the timestamped audit trail.
● OUT of scope
- ✕Packaging design and material selection — handled by your packaging team.
- ✕Trademark filing, IP, customs litigation.
- ✕Setting the company's packaging policy — decision of the COO / industrial leadership.
Named human reviewer
Every attestation published and every blocked item is reviewed by:
- Your Quality Manager — validates packaging conformity and signs the reference declarations.
- Damien Godard, founder of Taranis AI — validates structural decisions (cross-functional scope, tooling choice, missing data tradeoffs).
Review channel: weekly asynchronous review (email + traced comments) — no ephemeral Slack, no undocumented verbal decisions.
The single call
Two steps, one single call. No hidden commitment. The AI does the bulk; your Quality Manager keeps control.
Step 1 — 1-hour diagnosis
Where do you stand?
- · Review of your current packaging referential
- · Identification of exposed SKUs (PFAS, BPA, ratio)
- · Consolidated compliance score
- · Prioritized action plan for 08/12/2026
Deliverable: 4-page note, risk map, exposed SKU list.
Free if you take the pilot
Step 2 — 4-week pilot
Ongoing maintenance
- · Deploy collectors (suppliers, ERP)
- · Automated audit on a reference sample
- · Generation of declarations of conformity
- · Weekly human review: Quality Manager + Damien
Deliverable: operational EU register + audit trail.
Fixed-price pilot, quoted after diagnosis
4 weeks · no commitment · priced after the diagnosis
Other regulatory verticals
Taranis AI's compliance offer covers the full 2026-2027 European perimeter. Every role sheet starts from the same promise: a supervised AI agent + a named human reviewer.
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Battery Passport Assistant
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Real-Time Carbon Audit (CBAM)
Dynamic carbon traceability at SKU level to anticipate CBAM.
EU AI Act Compliance
Inventory, risk classification, high-risk system documentation.
Read also: our PPWR and AI Act guides
Pour approfondir la réglementation de référence de cette fiche rôle.