Industry association · Germany · EU Transparency Register 103122495301-83
3
positions filed
in the 326 files tracked
2
legislative files
of 326 tracked
3
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 #598 by legislative files engaged — a count of participation, not a measure of influence.
Self-declared to the EU Transparency Register (snapshot 30 Aug 2026).
Register category
Trade and business associations
Registered as
Bundesverband Medizintechnologie (BVMed)
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.
Work at Bundesverband Medizintechnologie | BVMed e.V.? so we know who speaks for it.
Their record over time
Bundesverband Medizintechnologie | BVMed e.V. filed 3 positions between 4 Oct 2025 and 14 Jul 2026, across 2 of the 326 legislative files tracked here, attaching a full position paper 3 times.
The targeted revision of the EU Medical Devices Regulation (MDR) is a crucial opportunity to make the European regulatory framework for medical devices more innovation-friendly, efficient and workable again, without compromising the high level of patient safety.
Filed in German · English published by the European Commission
The Bundesverband Medizintechnologie e.V. (BVMed) fully welcomes the European Commission’s ambition to streamline and future-proof the legal framework by reducing administrative burdens and increasing predictability and cost-effectiveness, while maintaining a high level of public health and patient safety, thereby contributing to the original objectives of the Regulations.
Filed in German · English published by the European Commission
Stellungnahme Verordnung über Biozidprodukte – Bewertung März 2026 Vorbemerkung Die Biozidprodukteverordnung (BPR, Verordnung (EU) Nr. 528/2012) ist ein zentrales Regelwerk für den Binnenmarkt, das seit 2013 die Zulassung und Verwendung von Biozidprodukten in der EU regelt.
Filed in German · English published by the European Commission
Opening of the attached position paper · the full paper is on the Commission’s record (source link above)
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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.
Everything on this page comes from Bundesverband Medizintechnologie | BVMed e.V.’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.