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Andermatt France

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.

2
positions filed
in the 665 files tracked
2
legislative files
of 665 tracked
0
with a full position paper
attached to a submission

Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.

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Their record over time

Andermatt France filed 2 positions between 31 Jan 2025 and 5 Mar 2026, across 2 of the 665 legislative files tracked here.

2025 · 1 filed2026 · 1 filed

What they argued

Evaluation of the Biocidal Products Regulationfiled 5 Mar 2026source

The presence of non-compliant biocidal products on the EU market raises significant concerns in terms of public health, environmental protection and the integrity of the regulatory framework established by the Biocidal Products Regulation (BPR). The BPR aims to ensure that biocidal products placed on the EU market meet strict safety, efficacy and risk assessment requirements.

Filed in French · English published by the European Commission

Plant Protection Products Labelling Regulationfiled 31 Jan 2025source

Andermatt France, a French distributor of Biocontrol products, IBMA Global’s position and its recommendations regarding the labeling requirements for PPPs. These requirements must be adapted and specifically appropriate for Biocontrol products. Andermatt France, a French distributor of biocontrol products, supported the position of IBMA as a whole and its recommendations on PPP labelling requirements.

Filed in French · English published by the European Commission

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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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Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.