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TEAM-NB

Industry association · Belgium · EU Transparency Register 731188910513-57

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 #786 by legislative files engaged — a count of participation, not a measure of influence.

3
declared lobbying FTE
self-declared
€200K+
declared costs / yr (floor)
2
EP accreditations
as declared to the register
2013
in the register since

Declares membership of

  • Team-NB is observer in MDCG working groups, HTA network.

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

Register category
Trade and business associations
Registered as
The European Association of Medical Devices – Notified Bodies (Team-NB)
Head office
Sprimont, Belgium

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 TEAM-NB engages with

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Their record over time

TEAM-NB filed 2 positions between 23 Jan 2026 and 8 Apr 2026, across 2 of the 326 legislative files tracked here, attaching a full position paper 2 times.

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 8 Apr 2026PDFsource

Team NB, the European Association of Medical Devices Notified Bodies, welcomes the opportunity to provide comments on the draft revision of EU Regulations. We support the Regulations objective of ensuring that only safe and effective devices are placed on the EU market, thereby safeguarding safety and public health while fostering innovation.

Implementing rules regarding requirements to be met by notified bodiesfiled 23 Jan 2026PDFsource

Team-NB, the European Association of Medical Devices Notified Bodies, welcomes the opportunity to comment on the draft Implementing Regulation amending AnnexVII MDR/IVDR. We support the goal of improving predictability, consistency and transparency in conformity assessment, but several elements of the draft raise significant legal, proportionality and feasibility concerns.

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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 TEAM-NB’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.