Becton Dickinson and Company (BD) supports the European Commission's efforts to revise the IVDR and MDR. We appreciate this opportunity to contribute to the call for evidence and share our perspective on recalibrating these regulations to better serve patients, healthcare systems, and the medical technology sector.
BD
Company · Belgium
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.
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Their record over time
BD 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 1 time.
What they argued
Becton Dickinson and Company (BD) welcomes the opportunity to respond to the public consultation on the draft Commission Implementing Regulation laying down uniform quality management and procedural requirements for conformity assessment activities carried out by Notified Body under the IVDR and MDR.
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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.
- MedTech Europe · 2 files in common
- EURAMET e.V. · 2 files in common
- TÜV-Verband e. V. · 2 files in common
- Cruelty Free Europe · 2 files in common
- Pharma Deutschland e.V. · 2 files in common
Showing 5 of 26.
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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.