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.
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.
MedTech Europe, the European trade association for the medical technology industry including diagnostics, medical devices and digital health welcomes the opportunity to provide comments on behalf of the medical technology industry to the European Commission on the Inception Impact Assessment regarding the revision of the Product Liability Framework.
The Italian Association of Young Lawyers has the honour to take part in the debate on product liability in order to supplement and/or repeal the current European Directive 85/374/EEC. First, the definition of a defective product (in Article 6 of the proposal) appears to be generic, since it does not provide objective parameters for the assessment, or the reference to point (h) of that article.
Filed in Italian · English published by the European Commission
As per the document attached that provides MedTech Europe more detailed feedback, we welcome the opportunity to provide feedback to the proposed revision of the EU Product Liability Directive (85/374/EEC) (PLD).
AIGA, the Italian Association of Young Lawyers, has always been particularly positive and interested in the technological development of the application of Artistic Intelligence, taking care to play an active role in stimulating the legal debate surrounding it, in order to ensure legal certainty and at the same time encourage the wider use of this instrument.
Filed in Italian · English published by the European Commission
MedTech Europe is the European association of medical technology manufacturers, including digital health products that fall under the scope of our sectoral regulations, some of which would fall under the scope of the proposed Artificial Intelligence Liability Directive (AILD).
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