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EUR

EUROM

Industry association · Germany · EU Transparency Register 585778511937-68

2
positions filed
in the 326 files tracked
2
legislative files
of 326 tracked
2
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 1205 trade and business associations on this site, they rank #698 by legislative files engaged — a count of participation, not a measure of influence.

0.5
declared lobbying FTE
self-declared
€10K+
declared costs / yr (floor)
0
EP accreditations
as declared to the register
2013
in the register since

Declares membership of

  • FPP4EU Collaboration Platform: https://www.fpp4eu.eu/news-and-events/events/
  • Umbrella Project

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

Register category
Trade and business associations
Registered as
European Federation of High-tech Industries (eurom)
Head office
Berlin, Germany

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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Follow the files EUROM engages with

One email on Tuesdays when a new position is filed on these 2 files, from EUROM or from anyone else on them. Only when there is something new.

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Their record over time

EUROM filed 2 positions between 6 Oct 2025 and 23 Jan 2026, across 2 of the 326 legislative files tracked here, attaching a full position paper 2 times.

2025 · 1 filed2026 · 1 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 Oct 2025PDFsource

EUROM welcomes the opportunity to provide feedback on the targeted revision of the EU rules for medical devices (MDR) and in vitro diagnostics (IVDR). This revision should aim to reduce bureaucratic burdens, strengthen governance and accountability, lower costs, foster competition and innovation, support small and medium-sized enterprises (SMEs), ensure consistency with horizontal legislation, and address future…

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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 26.

Is this your organization?

Everything on this page comes from EUROM’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.