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NBCG-MED

Other · Belgium · EU Transparency Register 482645249107-28

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 145 other organisations on this site, they rank #55 by legislative files engaged — a count of participation, not a measure of influence.

1.5
declared lobbying FTE
self-declared
—
declared costs / yr (floor)
0
EP accreditations
as declared to the register
2023
in the register since

Declares membership of

  • TeamNB - Association of Notified Bodies - https://www.team-nb.org/

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

Register category
Other organisations
Registered as
Notified Body Coordination Group - Medical Devices (NBCG-Med)
Head office
Amsterdam, Netherlands

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

NBCG-MED filed 3 positions between 6 Oct 2025 and 15 Apr 2026, across 2 of the 326 legislative files tracked here, attaching a full position paper 3 times.

2025 · 1 filed2026 · 2 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 15 Apr 2026PDFsource

Notified Bodies Coordination Group for Medical Devices (NBCG-Med) welcomes European Commissions initiative to address identified challenges in the implementation of Regulations (EU) 2017/745 and 2017/746 (MDR/IVDR) through a targeted revision.

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

NBCG-Med Summary for EU COM Survey Submission NBCG-Med fully supports the objectives of the EU MDR and IVDR regulations to establish a robust, transparent, and sustainable framework that ensures high safety standards while fostering innovation.

Implementing rules regarding requirements to be met by notified bodiesfiled 21 Jan 2026PDFsource

The EU NB feedback is summarised in slides attached. In summary, our top priorities are: 1. Article1: Quotations There is no reliable mechanism for NBs to confirm SME status, adding administrative burden. SME status should be validated and recorded in EUDAMED during user registration, providing a transparent and consistent verification process for all stakeholders, including NBs. 2.

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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.

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Everything on this page comes from NBCG-MED’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.