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GuidelinesRegulatory updates2026.09.23

PPWR for Exporters to the EU: Packaging and Documents to Review First

If you export products to the EU, packaging needs its own review alongside product certification. This guide explains the scope of PPWR, current obligations and phased application dates, and the documents to request from suppliers. It also introduces CLARE Partners' pilot consulting project for three Korean exporters.

Key takeaway — PPWR concerns more than packaging manufacturers. Companies exporting products to the EU should first establish what packaging they supply, who is responsible for it, and which documents support it.

PPWR is the EU Packaging and Packaging Waste Regulation, Regulation (EU) 2025/40. Its general application began on 12 August 2026. Individual obligations do not all begin on the same date, however. Companies need to distinguish requirements that already need attention from future changes to packaging design and labeling.

Is your product in scope? Start with the packaging

Cosmetic containers and individual cartons, pouches for household products, cushioning and shipping boxes for electronics, and protective packaging for medical devices can all be relevant. PPWR is not limited to a particular industry or to plastics. Packaging supplied to the EU market needs to be reviewed across a broad range of materials and uses.

Start with one representative export product. Identify its sales packaging, which reaches the consumer; grouped packaging, which brings several products together; and transport packaging, including boxes and pallet packaging. An item that functions as part of the product needs a separate assessment of whether it qualifies as packaging in the first place.

Next, review the supply arrangement. Roles differ depending on whether the product is sold under your own brand or made under contract, who the EU importer is, and how and in which countries the product is sold. A manufacturer or importer under PPWR must not be treated as synonymous with a producer under extended producer responsibility (EPR).

Separate current obligations from future preparation

Avoid blanket conclusions such as “we have until 2030” or “all packaging must change now.” The table below is not an exhaustive list of obligations. It sets out key dates to help prioritize your preparation.

Area to review How to interpret the application date
General application and economic operator obligations General application began on 12 August 2026. Review relevant obligations, including roles, traceability, technical documentation, and EU declarations of conformity, against the requirements currently applicable.
Recyclability The basic recyclability principle already applies. Distinguish this from the new design-for-recycling and grading framework, which applies from 1 January 2030 or 24 months after the relevant delegated act enters into force, whichever is later.
Recycled content in plastic packaging From 1 January 2030 or three years after the relevant implementing act enters into force, whichever is later. Percentages, calculation methods, and exceptions vary by packaging type; one percentage does not apply to all packaging.
Packaging minimization The new requirements in Article 10 apply from 1 January 2030. Existing requirements and transitional provisions still need to be checked before then, so start by documenting why the packaging's weight and volume are needed to protect the product.
Harmonized material labeling The harmonized material label under Article 12(1) applies from 12 August 2028 or 24 months after the relevant implementing act enters into force, whichever is later. This does not postpone other current labeling and identification obligations.

Actual assessments must also take account of packaging-specific exceptions and the latest follow-up legislation. In particular, the basic recyclability principle, the new assessment framework, and the transition dates for the relevant conformity assessment procedure should not be reduced to a single date. Use Articles 6, 7, 10, 12, 15, and 71 of PPWR and the Commission's implementation guidance as the basis for your review.

Start with a packaging component list

Photos alone may not reveal which documents are missing. Compiling the following information for the same product and packaging version makes it easier to identify what to request from suppliers. This is a practical checklist for a preliminary review, not a prescribed statutory form.

Documents and information to prepare What to check
Product and export route Product name and model, EU countries of sale, brand owner, manufacturer, and EU importer
Packaging components and photos The function of each component, such as the container, closure, label, individual carton, cushioning, and transport box
Materials, weight, and dimensions Resin type, composite materials, coatings, adhesives, each component's weight and dimensions, and whether components can be separated
Supplier evidence Specifications, material information, relevant test data, and evidence of recycled content and its scope where used
Design and protective performance Why the packaging is needed, including protection against breakage and leakage, storage conditions, and maintenance of sterility where relevant
Labeling and change history Current labels and identification information, drawing versions, packaging change dates, and the person responsible for preparing and updating records

Even a single cosmetic product may have a container, pump, label, and paper carton that need to be considered as separate components. A supplier's description of “eco-friendly packaging” does not establish each component's material, recyclability, or supporting evidence. Connect what each document demonstrates with the component it covers.

A gap analysis should go beyond a list of nonconformities

Missing evidence does not automatically establish that packaging performance is noncompliant. Conversely, if a legally required document is missing, the documentation obligation needs a separate review. Classifying findings into four categories makes follow-up work easier to assign.

  • Verified: The applicable requirement is linked to supporting evidence.
  • Further evidence needed: Additional support is needed, such as supplier confirmation or test data.
  • Design or operational review: The packaging configuration, labeling, or management procedures may need changes.
  • Preparation for phased requirements: Work is needed for future application dates and follow-up legislation.

For each item, record the applicable requirement, documents available, documents missing, responsible person, and next action. This turns a broad instruction to “review PPWR” into specific tasks: purchasing requests supplier documents, development reviews packaging design, and the export team checks arrangements with EU trading partners.

How CLARE Partners supports your preparation

CLARE Partners works with Korean licensed administrative agents (haengjeongsa) who have practical PPWR experience to support Korean exporters with applicability reviews and compliance preparation. The service covers companies exporting packaged products to the EU, including cosmetics, household products, and electrical and electronic products, as well as medical devices.

  1. Define the scope: Identify the representative product, packaging components, EU sales route, and relevant economic operators.
  2. Review applicability: Map the relevant requirements, exceptions, and application dates for each type of packaging.
  3. Assess the current position: Compare documents already available with those that need to be obtained from suppliers.
  4. Conduct a gap analysis: Distinguish missing evidence from issues requiring improvement review, and set priorities.
  5. Set out next steps: Identify the evidence and documents needed and the actions to take next.

The intended outputs are an applicability review matrix, a packaging inventory, a list of missing or incomplete documents, and a prioritized action plan. Specific deliverables and the depth of review will be agreed before work starts, based on the number of products, packaging complexity, and availability of documents. If further implementation support is needed, it can be arranged under a separate scope.

PPWR pilot consulting: applications open for three companies

This pilot is an initial project to assess the current state of packaging for EU exports and set out practical next steps together. It will also help build practical experience for a broader service offering. Company names and review findings will only be disclosed externally within the scope of separate consent.

We welcome interest from Korean companies that:

  • Already export to the EU or have a concrete export plan.
  • Can select a representative product and its packaging configuration, and work with us to review the relevant documents.
  • Need to respond to packaging information requests from EU trading partners or agree improvement tasks with suppliers.

We will review applications, discuss the scope and feasibility of obtaining documents, and then select three companies. Applying first does not guarantee a place. CLARE Partners also plans to approach companies with relevant needs and work with them on their preparation.

Pilot pricing will be offered to the three selected companies, with the initial assessment scope defined to keep costs to a minimum. Detailed fees and included services will be provided individually after an inquiry. Additional testing, packaging redesign, separate registration or agency services, and longer-term compliance support are not automatically included in the pilot; their necessity and costs will be agreed separately.

Share these four details when you contact us

Please provide your company and product name / EU export destinations and current status / packaging photos or a description of the components / a list of the documents you currently hold. You do not need to send all your detailed technical information or trade secrets at the outset.

Ask about joining the PPWR pilot — select “Other” under Topic and write “PPWR pilot participation inquiry” on the first line of your message. You can also call 070-7954-1254.

The first goal of PPWR preparation is to establish which requirements your company needs to review and what evidence supports those assessments, before rushing into packaging changes. Start with the packaging for one representative product together with CLARE Partners.

Official sources and review date

Reviewed on 23 September 2026. This article provides general practical guidance and does not replace a conformity assessment for an individual product or its packaging. Actual obligations must be reviewed in light of the packaging type, supply arrangement, countries of sale, and legislation applicable at the time.

Frequently asked questions

Q. Do we need to review PPWR even if we do not manufacture packaging?
Yes. Packaged products supplied to the EU market also need to be reviewed. Specific obligations depend on the packaging configuration, own-brand or contract manufacturing arrangements, the relationship with the EU importer, and the countries of sale. Requesting documents from packaging suppliers and establishing your company's legal role should go hand in hand.
Q. Does obtaining a PPWR certificate complete our compliance work?
PPWR should not be understood as a uniform procedure for obtaining third-party certification. Each operator needs to identify its obligations, including assessing conformity with the applicable requirements, preparing technical documentation, and drawing up an EU declaration of conformity. An existing CE marking for the product or a raw material certificate does not, by itself, demonstrate PPWR compliance for the packaging as a whole.
Q. Is medical device packaging excluded from PPWR?
Medical devices are not excluded as a whole. Some packaging is exempt from specific obligations, such as recyclability or recycled content requirements. Exceptions therefore need to be reviewed article by article, based on the packaging's function and configuration and the applicable product legislation. Packaging needed for product safety and sterility must not be reduced without proper justification.
Q. Can we inquire about the pilot if our documents are incomplete?
Yes. Start by sharing your product name, EU export destinations, packaging photos, and a list of the documents you currently hold. We will review the scope and the feasibility of obtaining the necessary documents before discussing participation and fees. You do not need to submit all your trade secrets or detailed technical information with the initial inquiry.

Just send the product details.
We do the reviewing.

We pre-review device class, required pathway, and data readiness free of charge, and reply within 1 business day. No sign-up.