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UL Solutions

Company · United States · EU Transparency Register 170568828821-78

7
positions filed
in the 326 files tracked
7
legislative files
of 326 tracked
5
with a full position paper
attached to a submission

Counts here are a floor, never a total: they cover the 326 consultation files tracked so far (29,503 submissions, mostly 2025–26), so an organization's real filing history is larger, not smaller.

Who they are

Among the 925 companies & groups on this site, they rank #84 by legislative files engaged — a count of participation, not a measure of influence.

1.9
declared lobbying FTE
self-declared
€200K+
declared costs / yr (floor)
0
EP accreditations
as declared to the register
2017
in the register since

Declares membership of

  • UL Solutions and its subsidiaries are actively involved in international and regional associations such as but not li…
  • European Electrical Products Certification Association (ETICS)
  • Der Bundesverband Informationswirtschaft, Telekommunikation und neue Medien e. V. (Bitkom)
  • AmCham DK
  • Amcham France
  • Dansk Industri (DI)

Self-declared to the EU Transparency Register (snapshot 30 Aug 2026).

Register category
Companies & groups
Registered as
UL GmbH (UL Solutions)
Head office
Schwerzenbach, Switzerland
EU office
Brussels

Self-declared to the EU Transparency Register (snapshot 30 Aug 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.

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Their record over time

UL Solutions filed 7 positions between 14 Jul 2023 and 6 Jul 2026, across 7 of the 326 legislative files tracked here, attaching a full position paper 5 times.

2023 · 1 filed2024 · 1 filed2025 · 2 filed2026 · 3 filed

What they argued

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 6 Jul 2026PDFsource

UL Solutions, a global leader in applied safety science, welcomes the European Commission's intent to simplify the medical technology system through the revision of the EU MDR/IVDR. UL Solutions supports the European Commission's further intention to keep Notified Body oversight strong. We would like, however, to highlight some concerns regarding the proposed governance of Notified Bodies.

Digital Product Passport Registry (DPP)filed 27 May 2026source

UL Solutions feedback on the draft Implementing Regulation for the Digital Product Passport Registry We welcome the Commissions work to establish the Digital Product Passport (DPP) registry and its core components, including the API, semantic repository and secure access framework. We support in particular the objective of interoperability through a common semantic repository with publicly documented interfaces.

Amending certain Regulations as regards digitalisation and common specifications (Omnibus IV)filed 25 Aug 2025PDFsource

UL Solutions respectfully submits these comments in response to the proposed regulation regarding digitalization and standard specifications. This proposal suggests introducing common specifications for accreditation standards within Regulation (EU) No. 765/2008. We believe this is unnecessary, as the existing harmonized standards for conformity assessment bodies are already fully adequate and effective.

Carbon footprint methodology for electric vehicle batteriesfiled 28 May 2024PDFsource

UL Solutions welcomes the opportunity to give feedback on the draft delegated act laying down the methodology for calculating and verifying the life-cycle carbon footprint of electric vehicle batteries, as required by the EU Battery Regulation.

Restriction on CMRs in childcare articlesfiled 4 Jun 2026source

UL Solutions feedback on the draft Regulation on Childcare articles restriction on substances classified as carcinogenic, mutagenic or toxic for reproduction (CMR) UL Solutions supports the objective of improving protection of children from exposure to substances classified as carcinogenic, mutagenic or toxic for reproduction (CMR) category 1A or 1B in childcare products.

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Turns up on the same files

Organizations that also filed on at least two of the same consultations. A shared interest in the same dossiers — not evidence of coordination, and we do not suggest any.

Showing 5 of 109.

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Everything on this page comes from UL Solutions’s own submissions to the European Commission — we have added nothing and interpreted nothing. If something is wrong or out of date, email info@policyspeak.com and we will correct it. If you are an individual named in a record, our privacy policy sets out your rights to correction, objection and removal.

Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.