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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.

HAP
2
files engaged
of 583 tracked
2
positions filed
in those 583 files
1.5
declared FTE
self-declared
1
EP accreditations
as declared to the register

Declared costs: €100K+ a year · in the register since 2016

Files both filed on (2)

Medicinal products for human use · Revision of the EU legislation on medicines for children and rare diseases

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

American Chamber of Commerce to the EU · filed 27 Apr 2021 · source

The American Chamber of Commerce to the EU (AmCham EU) is committed to the development of a regulatory environment which furthers the capabilities of European healthcare, improving accessibility and ensuring a crisis-resistant medicines regulatory system.

American Chamber of Commerce to the EU · filed 6 Nov 2023 · source

Introduction To be truly future proof and innovation friendly, the EU's proposed pharmaceutical package must address the blocs declining attractiveness for investment. We therefore urge EU co-legislators to secure globally competitive incentives for research and development (R&D) and avoid additional unnecessary administrative burdens on companies.

American Chamber of Commerce to the EU · filed 6 Nov 2023 · source

Introduction To be truly future proof and innovation friendly, the EU's proposed pharmaceutical package must address the blocs declining attractiveness for investment. We therefore urge EU co-legislators to secure globally competitive incentives for research and development (R&D) and avoid additional unnecessary administrative burdens on companies.

Hellenic Association of Pharmaceutical Companies · filed 8 Nov 2023 · source

The reform of the EUs pharmaceutical sector is a milestone of the European Health Union and a credible step in our collective step to pave the way towards a healthier, more resilient, and more equal Europe.SFEE fully supports the challenges of enhancing the availability and acceptability of medicines, all fostering a competitive innovation environment in Europe.

Filed in Greek · English published by the European Commission

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

Hellenic Association of Pharmaceutical Companies · filed 5 Jan 2021 · source

Hellenic Association of Pharmaceutical Companies (SFEE) members are committed to ensuring that unmet needs are addressed and that available treatments reach all European patients. Children and rare disease (RD) patients have greatly benefited from the progress achieved through the Paediatric & Orphan Regulations.

American Chamber of Commerce to the EU · filed 6 Jan 2021 · source

Representing American companies operating in the EU, AmCham EU is well aware of the differences and respective strengths of innovation ecosystems on both sides of the Atlantic. The options laid out in the inception impact assessment (IIA) risk undermining an EU framework that has proven largely successful, rather than preserving the EU’s strengths and incorporating learnings from other regions.

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