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FEP

FEPPD

Other · France · EU Transparency Register 888641713561-86

2
positions filed
in the 665 files tracked
1
legislative file
of 665 tracked
2
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 #1185 by legislative files engaged, a count of participation, not a measure of influence.

2.5
declared lobbying FTE
self-declared
€50K+
declared costs / yr (floor)
0
EP accreditations
as declared to the register
2014
in the register since
Register category
Trade and business associations
Registered as
Fédération européenne et internationale des Patrons Prothésistes dentaires (FEPPD)
Head office
Brussel, Belgium
EU office
Mechelen

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

FEPPD filed 2 positions between 26 Jun 2026 and 14 Jul 2026, across 1 of the 665 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 14 Jul 2026PDFsource

Following the submission of FEPPD's response to the European Commission's public consultation on the targeted revision of Regulations (EU) 2017/745 (MDR) and 2017/746 (IVDR), further discussions within the FEPPD network have identified an additional issue which, in our view, deserves consideration during the legislative process.

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 26 Jun 2026PDFsource

FEPPD respectfully submits the attached position paper in response to the European Commission's public consultation on the targeted revision of Regulations (EU) 2017/745 and 2017/746. The attached document contains FEPPD's detailed observations and recommendations, based on the practical experience of European dental laboratories manufacturing custom-made medical devices.

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Is this your organization?

Everything on this page comes from FEPPD’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.