From 12 August 2026, every item of packaging placed on the EU market must have a Declaration of Conformity (DoC) and technical documentation compliant with Regulation (EU) 2025/40 (PPWR). In our audit practice, however, we see companies start with a declaration template and only then ask: for exactly which packaging, in which sales stream, and who should actually sign it? This is the reverse of the correct order, as the traceability of packaging under the PPWR is fundamental. Each batch of packaging must be unambiguously linked to its manufacturer, material composition, test reports and – a point that is often overlooked – the sales model through which the packaging enters the market.
16.07.2026
The PPWR applies to packaging the logic known from EU product legislation. Article 15 obliges the manufacturer to ensure identification of the packaging type and batch and to indicate its name and address on the packaging or in a data carrier (e.g. a QR code). Annex VII (Module A) requires technical documentation describing the materials, the design and the evidence of compliance with Articles 5–12, while Article 39 together with Annex VIII requires a Declaration of Conformity that unambiguously identifies the packaging it covers.
Suppliers of packaging and components (canisters, closures, labels) are obliged to provide the recipient with all information necessary to demonstrate compliance (Article 16) – but their declarations do not replace the responsibility of the entity that places the final, filled unit on the market under its own brand.
The Declaration of Conformity is drawn up for a packaging type – not for every single item (Annex VIII point 2: an identification number unambiguously indicating the packaging covered by the declaration). Responsibility, however, reaches deeper: Article 15 requires the packaging to bear a type, batch or serial number enabling its identification, and Module A (Annex VII) obliges the manufacturer to ensure that every unit from series production remains in conformity with the technical documentation.
Whenever the raw material, the design, a component supplier or the legal requirements change, conformity must be reassessed and the DoC updated (Article 39).
The PPWR does not require the manufacturer’s logo to appear on every individual unit of empty packaging. However, it does require that the documentation makes it possible, at any time, to link a batch of packaging to its manufacturer and to the batch of the product placed on the market. Without this, the DoC cannot be verified.
The second dimension of traceability concerns extended producer responsibility. Under Article 3(1)(15) PPWR, the “producer” for EPR purposes is whoever makes packaging or a packaged product available for the first time on the market of a given Member State. This role therefore changes with every sales stream:
In such a situation, the distributor is the ‘manufacturer’. It is the distributor who registers, reports tonnages and pays the ROP fees. The importer from Poland has no obligations in this country. However, they should confirm the division of roles in the contract and provide the distributor with details of the weights and materials of the packaging. Examples:
in each of these cases the wholesaler, the chain and the distributor act as distributors who are the first to make the product available on their market, and it is they, as “producers” within the meaning of Article 3(1)(15)(a), who bear the EPR obligations in the destination country.
he Declaration of Conformity does not follow the sales model – it is always drawn up by the manufacturer within the meaning of Article 3 PPWR, i.e. the entity placing the packaging or packaged product on the market under its own brand (here: the Polish manufacturer); the distributor is only obliged to check that the declaration exists (Article 19). More on the roles involved in signing declarations: Who signs the PPWR Declaration of Conformity?
n that case the company itself becomes the “producer” there: it must appoint an authorised representative for EPR (Article 45), register in the national producer register (Article 44) and pay the fees. Examples:
The authorised representative for EPR (Article 45) does not take over the Declaration of Conformity – the DoC is still drawn up and signed by the manufacturer. A separate role is the representative under Article 17 PPWR, who may draw up the DoC and keep the documentation on behalf of a non-EU manufacturer. We describe the difference between these two roles here: The Authorised Representative under the PPWR.
| Without identifying every packaging item in every sales stream, obligations cannot be assigned correctly. We see the consequences regularly – the DoC is drawn up by the wrong entity or covers the wrong scope of products, EPR fees go to the wrong country or are paid twice, and during an inspection it is impossible to demonstrate which packaging batch comes from which manufacturer. |
This is not a problem of the future. Already today, a Polish manufacturer selling B2C abroad (own online shop, marketplaces, deliveries straight to users) pays EPR fees in countries where the rates are in force and enforced, including:
Failure to register in these systems means the risk of penalties and sales blocks – marketplaces verify registration numbers. More on the fee mechanism and eco-modulation: PPWR and EPR fees.
We therefore recommend starting your preparations not with the declaration template, but with an inventory. The obligation to identify items stems directly from the Regulation. Article 15 of the PPWR requires the identification of the type and batch of packaging, whilst Annex VII requires technical documentation describing each component of the packaging unit. This is where the linking and mapping of data in the context of the PPWR begins. It is best to do this straight away in the context of the ROP as well. The same data on components, materials and weights will later be used to populate the declaration of conformity, tonnage reports and the calculation of fees in the destination countries.
The table below sets out our proposal for the minimum scope of data that should be collected for each type of packaging. This data should be updated for each series (batch). This is in line with the principle: declaration – by type; traceability – down to batch level.
| What data should be collected? | Why is it required? | Basis / purpose | Since when? |
| Packaging components and the material of each (container, closure, label, filler, tape, adhesive). | The DoC and technical documentation cover the entire packaging, including components that cannot be separated by hand. The supplier of each component provides the required data. | Art. 16, art. 38–39, annex VII–VIII. | 12 August 2026 |
| The character and type of packaging (unit, bulk, transport; single- or multi-material). | The data is required for EPR reporting. Multi-material designs may be assigned a lower recyclability class and incur higher fees. | Art. 6. | EPR – already today; Grades A-C: 1 January 2030 |
| The origin of each component (Poland, the EU, a third country). | It defines the role within the supply chain, identify the entity drawing up the DoC and the party responsible for compliance. | Art. 15 i 18. | 12 August 2026 |
| Test results for heavy metals, including test dates. Sales streams (country by country, B2B/B2C). | It confirms compliance with substance limits and form part of the technical documentation. | Art. 5 (4). | Heavy metals – already today;
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| Test results for PFAS, including test dates. Sales streams (country by country, B2B/B2C). | Reagard the packaging intended for food contact. It confirm compliance with substance limits and form part of the technical documentation. | Art. 5 (5). | PFAS – 12 August 2026 |
| Sales streams country by country: B2B (to a distributor) or B2C (to the end user). | It enables the identification of the EPR manufacturer, the obligation to appoint an authorised representative, and the allocation of responsibilities in contracts. | Art. 3 (1 & 15), art. 45. | EPR – already today; PPWR – 12 August 2026 |
| Estimated EPR fees for each stream. | It enables the estimation of costs and an assessment of the cost-effectiveness of changes to the packaging design. | Cost planning and eco-modulation. | It’s worth getting started today |
It is worth thinking about the next stages now. For some organisations, it may also be important to carry out an assessment covering:
The declared recyclate must be demonstrable (mass balance, certification e.g. RecyClass / EN 15343), and without a certified supply chain it does not count towards the result.
Obligation: minimum levels from 1.01.2030 (Article 7); in some countries recyclate already lowers EPR fees today.
⭢ Find out how to verify the recycled content.
The packaging recyclability grade (A/B/C) will be the basis of eco-modulation and a direct tool for reducing EPR fees; not only finished packaging is assessed, but also its elements – a canister, closure, label, film or laminate can be assessed separately.
Obligation: recyclability grades become a requirement from 1.01.2030, but RecyClass Recyclability certificates are valid for 3 years – by seeking certification as early as, say, late 2027, you write it directly into the 2030 obligations and gain time for any packaging design changes.
Silk Road Certification supports companies in identifying the type of sale, their role in the supply chain and the packaging components. We help determine who is the manufacturer drawing up the declaration of conformity, and who is the ‘manufacturer’ under the ROP responsible for the fees. As a result, the certification serves as valuable evidence supporting the declaration of conformity (DoC). That is why we do not start with a form template, but with the supporting documents on which the Declaration of Conformity should be based.
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