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.
Company · France
Industry association · Belgium
Declared costs: €1.5M+ a year · in the register since 2016
Medicinal products for human use · 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.
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.
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.
MaaT Pharma · filed 8 Nov 2023 · source
*Introduction MaaT Pharma, a clinical-stage biotechnology company committed to treating cancer and graft-versus-host disease (GvHD), a serious complication of allogeneic stem cell transplantation. The companys Microbiome Ecosystem Therapies are produced through a standardized cGMP manufacturing and quality control process to safely deliver the full diversity of the microbiome (eg: the entire microbiome ecosystem) in…
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.
MaaT Pharma · filed 8 Sept 2022 · source
Introduction We acknowledge the European Commission’s proposal on standards of quality and safety for Substances of Human Origin (SoHO) for human application and welcomes the opportunity to participate to this consultation.
MaaT Pharma · filed 8 Sept 2022 · source
We acknowledge the European Commission’s proposal on standards of quality and safety for Substances of Human Origin (SoHO) for human application and welcomes the opportunity to participate to this consultation. This will increase EU harmonization on protection of the rights and safety of SoHO donors and recipients and create a regulatory status and common rules for SoHOs currently not regulated neither as medicinal…
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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