The European Commission clarifies implementation in a second version of its FAQ
August 10, 2026

Joaquim Alves Gaspar, CC BY-SA 3.0 <http://creativecommons.org/licenses/by-sa/3.0/>, via Wikimedia Commons
To accompany the entry into application of the PPWR, the European Commission published in early August 2026 the 2nd edition of its Frequently Asked Questions (FAQ), updating the March 2026 version and complementing its June 2026 Guidance Document. Questions marked “NEW!” or “UPDATED” help users quickly identify clarified points. This document is not legally binding, but it reflects the Commission’s interpretation of the regulation and provides guidance for the approach of companies and national market surveillance authorities.
Key points
- The FAQ updates and completes the March 2026 version, with questions marked "NEW!" or "UPDATED".
- A major part of the updates focuses on manufacturers’ obligations: stock management, language of the declaration of conformity, delegation to third parties, importers.
- The Commission clarifies how to manage packaging already produced or in stock as of 12 August 2026.
- The Commission recommends a gradual enforcement: warning and time for correction prior to any sanction.
I. Context
The PPWR regulation entered into force on 11 February 2025, with the first binding deadline set for 12 August 2026 (restrictions on hazardous substances, manufacturers’ documentary obligations). To provide guidance to stakeholders, the Commission updated its FAQ in a second edition, building on its June 2026 Guidance Document, which remains the reference for interpretation of the regulation.
II. Management of packaging already produced or in stock as of 12 August 2026
The Commission confirms that packaging produced or in stock before 12 August 2026, but not yet placed on the market, does not need to be destroyed, remanufactured or relabelled. To meet the requirements for identification and manufacturer name/address (Art. 15(5) and 15(6)), an accompanying document can be used rather than direct marking on the packaging.
III. Other key clarifications
- Language of the DoC: The Declaration of Conformity must be drafted in the language(s) required by the Member State where the packaging is placed on the market (Art. 39(2)).
- Delegation to a third party: The manufacturer can entrust certain tasks (maintenance of documentation, availability to authorities) to a third party, but legal responsibility remains fully with the manufacturer and cannot be transferred contractually.
- Traceability: Article 15(5) does not require unit-by-unit marking; identification by batch or production type may suffice in most cases. For example, standardised and common packaging, such as adhesive tape or generic plastic bags purchased from suppliers, are usually traceable at the batch level, not individually.
- Importers: They must verify that the non-EU manufacturer has completed the conformity assessment and prepared the declaration of conformity before importing.
IV. A gradual control approach
In cases of identified non-compliance, the European Commission advises market surveillance authorities to first request that the operator correct the situation, taking a supportive approach rather than immediate sanction. Only in cases of persistent non-compliance may more restrictive measures (ban, recall, withdrawal) be taken.
A point of vigilance: who is the “manufacturer”? Beyond these clarifications, the FAQ provides guidance to analyse a preliminary question: who, within their supply chain, actually assumes the role of manufacturer under the PPWR? (Re)verifying this qualification remains a key priority for many operators.
V. In practice
- Ensure clarity about who, within the supply chain, holds the status of manufacturer.
- Check whether packaging in stock as of 12 August 2026 requires an accompanying document rather than physical marking, and ensure these documents can be unambiguously linked to the relevant packaging batches.
- Anticipate the required language version of the DoC according to the destination Member States.
- Document steps taken with recalcitrant suppliers to demonstrate “best efforts” in the event of a control.
This article provides a general overview of the applicable European regulatory framework. It does not constitute legal advice and should not be used as a substitute for legal analysis adapted to your company’s specific situation.