PPWR & regulatory transition for packaging
medicom is here to help: a practical and comprehensive guide

The European PPWR (Packaging and Packaging Waste Regulation) is gradually being implemented across the European Union. It aims to promote the circularity of packaging, encourage its recyclability, reduce waste and harmonise the rules applicable within the European market.
Against this backdrop, Medicom is actively preparing for this regulatory transition alongside its industrial partners and packaging suppliers.
What you’ll learn in this article:
- How is Medicom preparing for the transition?
- How is the regulatory framework gradually evolving?
- Information that Medicom may gradually disclose.
- Frequently Asked Questions (FAQ).

How is Medicom preparing for the transition?
Our aim is to support you by providing clear, reliable and regularly updated information as European implementing legislation is published and supplier data is consolidated.
We are committed to providing you with transparent information about the packaging of your Medicom products, whilst taking into account the regulatory timetable and matters that are still being clarified at European level.
| Regulatory monitoring | Supplier collection | Customer information |
|---|---|---|
| Monitoring of PPWR requirements and the associated implementing regulations. | Consolidation of data available from our industrial partners. | Relevant information will be made available in stages, depending on the products and packaging concerned. |
How is the regulatory framework gradually evolving?
Certain official methodologies, in particular those relating to:
- a detailed assessment of recyclability;
- minimising packaging;
- harmonised labelling,
remain subject to implementing regulations or European delegated acts.
Medicom will update the information provided as and when it is published. The data will be expanded gradually in line with changes to the European regulatory framework and the availability of supplier documents.
The information that Medicom may gradually disclose
Depending on the products, ranges and information available from our suppliers, Medicom may gradually provide the following:
- the nature and composition of packaging materials;
- the weight of the main packaging components;
- declarations relating to regulated substances where relevant, including PFAS, heavy metals or substances of concern;
- information relating to recyclability, based on the available data and methodologies;
- the technical documentation or supplier certificates available for the packaging in question.

Frequently Asked Questions (FAQ)
Not all skin reactions are the same: some are allergic, whilst others are simply irritant. Specialists distinguish between three main types:
Is the PPWR already in effect?
The regulation is being phased in. Some requirements will apply from 12 August 2026, whilst others will be set out in further European legislation.
What information can I request from Medicom?
Depending on the relevant reference numbers, you can request the information available regarding:
- the supplier documentation available.
- the composition of the packaging;
- their weight;
- controlled substances;
- recycled content, where applicable;
- recyclability;
- the supplier documentation available.
Can Medicom provide a complete declaration of conformity right now?
Medicom is compiling the available information and documents. Full compliance will, in certain respects, depend on official methodologies that are still being clarified at European level.
Will the information be updated?
Yes. Medicom will regularly update the information provided as further European requirements are published and as it consolidates data from its suppliers.
Does this communication constitute a declaration of conformity?
No. This notice is for information purposes only. The relevant technical documents or declarations will be provided separately once they are available and relevant to the products in question.
Need any further information?
If you have any queries regarding the packaging of your Medicom products, please contact your usual sales representative.
Our teams will direct you to the relevant information based on the specific references.
This content is provided for information purposes only and does not constitute a declaration of product conformity or legal advice.






