Side by side
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.
NGO · Netherlands
Industry association · Belgium
Declared costs: €200K+ a year · in the register since 2010
European Open Digital Ecosystems · A European Health Data Space
Register facts self-declared (snapshot 2 Sept 2026); cost bands are floors. Shared files are shared attention, not evidence of coordination.
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.
EATRIS-ERIC · filed 2 Feb 2026 · source
This contribution presents the perspective of the EATRIS-CONNECT consortium on the European strategy for Open Digital Ecosystems, drawing on operational experience at the intersection of biomedical research, translational medicine, data, and AI.
ACT | The App Association · filed 3 Feb 2026 · source
ACT | The App Association (hereafter ACT) welcomes the opportunity to submit comments to the European Commissions consultation on the European open digital ecosystems initiative. ACT is a policy trade association for the small business technology developer community. Our members are entrepreneurs, innovators, and independent developers within the global app ecosystem that engage with verticals across every industry.
ACT | The App Association · filed 2 Feb 2021 · source
Please find attached comments of ACT | The App Association (Transparency Reg. # 7202951387754) on the European Commission’s Roadmap "A European Health Data Space" (Ref. Ares (2020)7907993). Anna Bosch Policy Associate ACT | The App Association (Transparency Reg. # 7202951387754) Rue de Trèves 45 B-1040 Brussels
EATRIS-ERIC · filed 27 Jul 2022 · source
EATRIS-ERIC is the European infrastructure for translational medicine, mandated by 14 European Members States to bring together resources and services for research communities to translate scientific discoveries into benefits for patients.
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