Academic / research · France · EU Transparency Register 264764996511-23
Counts here are a floor, never a total: they cover the 326 consultation files tracked so far (29,503 submissions, mostly 2025–26), so an organization's real filing history is larger, not smaller.
Among the 44 academic institutions on this site, they rank #12 by legislative files engaged — a count of participation, not a measure of influence.
Self-declared to the EU Transparency Register (snapshot 30 Aug 2026).
Self-declared to the EU Transparency Register (snapshot 30 Aug 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.
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INSERM filed 4 positions between 7 Oct 2025 and 15 Jun 2026, across 3 of the 326 legislative files tracked here, attaching a full position paper 2 times.
INSERM fully supports the European Commission’s proposal to strengthen the biotechnology and biomanufacturing sectors in the field of health. The Institute welcomes in particular the Commission’s commitment to tackle the fragmentation and regulatory complexity that are currently holding back the development of this sector in Europe.
Filed in French · English published by the European Commission
As a future user of the HealthDCAT-AP standard, INSERM would like to thank the Commission for giving us the opportunity to provide feedback on the amendments to Article 77. We would, however, like to draw attention to several points which currently raise questions regarding their implementation.
It is now widely recognized that biodiversity is being severely undermined by the massive use of pesticides, industrialization, soil artificialization, and global warming. The ever-increasing use of pesticides worldwide is particularly being called into question because products are authorized for market release based on tests that are inadequate or even flawed.
It is now recognised that biodiversity is being undermined in competition by the massive use of pesticides, industrialisation, soil lartificialisation and global warming. The use of pesticides, which is still growing worldwide, is particularly marked by the fact that products assessed with insufficient or defective tests have been authorised on the market.
Filed in French · English published by the European Commission
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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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