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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
4
positions filed
in those 583 files
2.1
declared FTE
self-declared
1
EP accreditations
as declared to the register

Declared costs: not declared · in the register since 2009

EUR
EuropaBio

Industry association · Belgium

15
files engaged
of 583 tracked
21
positions filed
in those 583 files
1.1
declared FTE
self-declared
4
EP accreditations
as declared to the register

Declared costs: €100K+ a year · in the register since 2009

Files both filed on (3)

Medicinal products for human use · Revision of the EU legislation on medicines for children and rare diseases · Compulsory licensing of patents in crisis situations

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

Health Action International (HAI) · filed 26 Apr 2021 · source

HAI welcomes the opportunity to provide feedback to the evaluation and revision of the general pharmaceutical legislation and appreciates the importance of the initiative taken by the European commission to update and adapt a keystone of the European Health Union.

EuropaBio · filed 27 Apr 2021 · source

The evaluation and revision of the general pharmaceutical legislation is the opportunity to create a future-proof, patient-oriented and leading life sciences and biotechnology sector in the EU. New biotechnology-derived vaccines and treatments have helped to tackle numerous life-threatening illnesses. Targeted cell and gene therapies and new mRNA platforms are paving the way for future treatments.

EuropaBio · filed 9 Oct 2023 · source

In the last 20 years, biotech transformed the pharmaceutical industry and enabled the development of breakthrough therapies that are live-saving or significantly improving quality of life of patients and their families. The development of biotech in Europe also continues to positively contribute to the regions economic well-being.

Revision of the EU legislation on medicines for children and rare diseases

Health Action International (HAI) · filed 21 Dec 2020 · source

Health Action International (HAI) welcomes the opportunity to contribute to the ‘Revision of the EU legislation on medicines for children and rare diseases’ and commends the European Commission for the thorough and comprehensive consultation process that is shaping the reform of legislation on this topic.

EuropaBio · filed 6 Jan 2021 · source

Developing medicines for children and rare diseases is a lengthy and complex undertaking. Much less is known about these illnesses when compared to more common conditions, meaning extensive research is required before scientists and researchers can seek to transform their ideas into potential treatments.

Compulsory licensing of patents in crisis situations

Health Action International (HAI) · filed 29 Apr 2022 · source

Health Action International (HAI) welcomes the step taken by the European Commission towards an enhanced use of Compulsory Licenses (CL) in EU territory; such measure will have a positive impact on access to medicines and health technologies, strengthening the ability of governments to fulfill the human right to health beyond crisis or exceptional circumstances.

EuropaBio · filed 28 Jul 2023 · source

The COVID-19 pandemic has shown the importance for Europe to have the right tools to respond to major health crises. The EU has already adopted several laws to improve its ability to respond to health emergencies and the coordination between the Member States.

Health Action International (HAI) · filed 29 Jul 2023 · source

The European Commission proposal COM(2023)224 and accompanying documents is an overdue step forward towards a more nuanced balanced between innovation and access as it aims to streamline and facilitate the use of Compulsory Licenses.

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