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Consultation participation and their own register declarations, side by side. Counts, not judgments — participation is not influence.

Counts here are a floor, never a total: they cover the 583 consultation files tracked so far (42,224 submissions, mostly 2025–26), so an organization's real filing history is larger, not smaller.

3
files engaged
of 583 tracked
3
positions filed
in those 583 files
1
declared FTE
self-declared
1
EP accreditations
as declared to the register

Declared costs: €200K+ a year · in the register since 2015

Files both filed on (3)

Medicinal products for human use · A European Health Data Space · Standards of quality and safety for substances of human origin intended for human application

Register facts self-declared (snapshot 2 Sept 2026); cost bands are floors. Shared files are shared attention, not evidence of coordination.

What each said, in their own words

Their opening passages on the files they share, verbatim and in filing order. We do not summarize, compare, or characterize positions — read them at source.

Medicinal products for human use

MedTech Europe · filed 26 Apr 2021 · source

As the association representing the medical technology sector, MedTech Europe welcomes the recognition in the inception impact assessment that pharma health solutions bring about technological advances, and the inclusion of the potential of the digital transformation of health and care.

United European Gastroenterology (UEG) · filed 28 Aug 2023 · source

United European Gastroenterology (UEG) is the leading non-profit organisation for excellence in digestive health in Europe and beyond. We promote science, research, education, quality of care and advocate to prevent and reduce health inequalities across Europe to achieve optimal patient care. We unite 17 Specialist Member Societies and 49 National Member Societies.

A European Health Data Space

United European Gastroenterology (UEG) · filed 3 Feb 2021 · source

United European Gastroenterology (UEG) is a professional non-profit organization combining all the leading European medical specialists and national societies focusing on digestive health. Together, we act as the united and trusted voice of European Gastroenterology, promoting science, research, education, quality of care. We aim at reducing health inequalities across Europe.

MedTech Europe · filed 3 Feb 2021 · source

MedTech Europe supports the project of the European Health Data Space (EHDS). The medtech industry is at the heart of the health data ecosystem. The industry’s digital health solutions annotate and enrich data to turn raw data into datasets of high value. Innovation in the development of new treatments and protocols is highly dependent on its ability to access and appropriately utilise health data.

MedTech Europe · filed 28 Jul 2022 · source

MedTech Europe welcomes the opportunity to provide feedback on the proposed European Health Data Space (EHDS) regulation, please find our full answer attached. • The EHDS regulation is meant to complement other EU laws, including existing sectoral and horizontal legislation.

Standards of quality and safety for substances of human origin intended for human application

MedTech Europe · filed 14 Dec 2020 · source

MedTech Europe - the European trade association for the medical technology industry including diagnostics, medical devices and digital health - welcomes the opportunity to contribute to the initial consultation regarding the revision of the Union legislation on blood, tissues and cells.

United European Gastroenterology (UEG) · filed 7 Sept 2022 · source

UEG Response to the EU Proposal for a Regulation on Blood, tissues and cells for medical treatments & therapies United European Gastroenterology (UEG) is a professional non-profit organization combining all the leading European medical specialists and national societies focusing on digestive health.

MedTech Europe · filed 8 Sept 2022 · source

MedTech Europe welcomes the Proposal for a Regulation on substances of human origin adopted by the European Commission in July 2022. We agree that the sector needs updated legislation, and the proposed text reinforces the rules for safety and quality. We are looking forward patients to having smooth access to products, the availability of which is uninterrupted on the European market.

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