Cécile Rousseau
July 15, 2024
ESPR: It’s time to take action!
Let’s take a closer look at the Ecodesign for Sustainable Products Regulation (ESPR). Although the new legislation comes first into force in 2027, we explain why it makes sense to get started straight away and share some tips to help you begin.
- Get familiar with key concepts: concepts such as circularity, carbon footprint, environmental footprint of products, eco-conception, CE marking framework and the safe and sustainable by design framework should be thoroughly understood and shared throughout different functions within the company and along the supply chain.
- Streamline data generation and management: this will be key, both inside the company and within the supply chain. The DPP and Life Cycle Assessment requirements demand high quality and reliable data to ensure useful outputs and mandatory transparency.
- Be aware of substances of concern: As defined in the ESPR, such substances must be considered when managing the product portfolio. The ESPR definition differs from that defined within the Biocidal Regulation (EU) 528/2012 and covers not only Substances of Very High Concern (SVHCs) under REACH (Registration, Evaluation, Authorisation, and restriction of CHemicals, (EC) 1272/2008), but a much wider range of substances. This confirms the importance of implementing a process to ensure the traceability of substances throughout the supply chain as already suggested in the context of other recent EU legal texts (e.g., the battery regulation).
- Consider recyclability: It is important to assess the potential impact substances within the product can have on recyclability of these products as well as their packaging.
- Take a holistic approach to product circularity and sustainability: Investigate the circularity and sustainability of the products put on the market; their content in recyclable materials and optimisation of this content, not only from the point of view of the packaging but also regarding raw materials and substances contained in the products itself (e.g. bio-sourced materials to be assessed in terms of resource consumption and the possibility to recover substances when the product is discarded etc.).
- Perform a second screen of the company’s product portfolio: The Delegated Acts will set product-specific thresholds for substances of concern and additional requirements in terms of recyclability.
- Revisit Digital Product Passports: The Delegated Acts will also set product-specific requirements for the content of the DPP. Requirements for new information should be quickly communicated throughout the supply chain, as the new requirements will enter into force 18 months after the Delegated Acts. Anticipation will be key.
Want to know more?
Cécile Rousseau
Principal, Health Sciences
Imani Hamilton
Senior Managing Consultant
Meera Cush
Senior Managing Consultant
+44 7812 494143