Team NB, as notified bodies association, welcomes the Commission's initiative to drive forward the simplification of the digital regulatory framework and reduce administrative costs for businesses as part of the Digital Omnibus.
TN
TEAM-NB
Industry association · Belgium · EU Transparency Register 731188910513-57
3
positions filed
in the 665 files tracked
3
legislative files
of 665 tracked
3
with a full position paper
attached to a submission
Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.
Who they are
Among the 1518 trade and business associations on this site, they rank #939 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 14 Oct 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 14 Oct 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.
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Their record over time
TEAM-NB filed 3 positions between 14 Oct 2025 and 8 Apr 2026, across 3 of the 665 legislative files tracked here, attaching a full position paper 3 times.
2025 · 1 filed2026 · 2 filed
What they argued
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.
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 61.
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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.