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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
  • Regulatory Update

Sustainability: EC Postpones EU Battery Regulation Due Diligence Policies

On July 30, 2025, the European Commission (EC) enacted Regulation (EU) 2025/1561 amending Regulation (EU) 2023/1542 regarding economic operators’ obligations concerning battery due diligence policies.

Different types of batteries next to each other

September 16, 2025

On July 30, 2025, the European Commission (EC) enacted Regulation (EU) 2025/1561 amending Regulation (EU) 2023/1542 regarding economic operators’ obligations concerning battery due diligence policies.

This Regulation postponed the implementation of due diligence obligations for economic operators from Aug. 18, 2025, to Aug. 18, 2027.

In addition, this Regulation also postponed the deadline to publish guidelines regarding due diligence requirements from Feb. 18, 2025, to July 26, 2026.

These postponements grant economic operators more time to comply with due diligence requirements for batteries placed on the EU market and facilitate the designation of notified bodies involved in verifying these requirements, which is taking more time than expected.

Official source

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Get connected with our sales team

UL Solutions helps manufacturers, retailers and brands stay informed in an evolving regulatory landscape so they can continue providing compliant products to their target markets.

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