*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…
MaaT Pharma
Company · France
not in the EU Transparency RegisterThis organization files on consultations without a register number, so its record here is built from its filings alone. Register facts — staff, costs, accreditations — are not available for it.
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.
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Their record over time
MaaT Pharma filed 3 positions between 8 Sept 2022 and 8 Nov 2023, across 2 of the 583 legislative files tracked here, attaching a full position paper 1 time.
What they argued
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.
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…
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Turns up on the same files
Organizations that also filed on at least two of the same consultations. A shared interest in the same dossiers — not evidence of coordination, and we do not suggest any.
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