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MH

ministry of health

Public authority · Spain

4
positions filed
in the 326 files tracked
3
legislative files
of 326 tracked
3
with a full position paper
attached to a submission

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.

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Their record over time

ministry of health filed 4 positions between 12 Mar 2025 and 2 Mar 2026, across 3 of the 326 legislative files tracked here, attaching a full position paper 3 times.

2025 · 1 filed2026 · 3 filed

What they argued

The European Ocean Actfiled 9 Feb 2026source

The Spanish Ministry of Health considers it appropriate to explicitly strengthen the integration of human health into maritime spatial planning and governance processes. While the European Ocean Act adequately addresses key aspects such as climate change, biodiversity loss and pollution, better consideration of the interlinkages between environmental pressures in marine and coastal environments and population health…

Filed in Spanish · English published by the European Commission

Evaluation of the Biocidal Products Regulationfiled 2 Mar 2026PDFsource

DIPARTIMENTO DELLA PROGRAMMAZIONE, DEI DISPOSITIVI MEDICI, DEL FARMACO E DELLE POLITICHE IN FAVORE DEL SERVIZIO SANITARIO NAZIONALE DIREZIONE GENERALE DEI DISPOSITIVI MEDICI E DEL FARMACO Ufficio 8 – Biocidi e cosmetici Viale Giorgio Ribotta, 5 - 00144 Roma PEC:[email removed] 4 March 2026 Response of the Italian Competent Authority to the Call for Evidence in the Evaluation of the Biocidal Product Regulation (BPR)…

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

Evaluation of the Biocidal Products Regulationfiled 24 Feb 2026PDFsource

IT COMMENTS ON THE REVISION OF EU BIOCIDAL PRODUCTS REGULATION NO. 528/2012 ARTICLE 5 Exclusion criteria TO AMEND PAR.1 AS FOLLOWS: […] (a) active substances which have been classified in accordance with Regulation (EC) No 1272/2008 as carcinogen category 1A or 1B; (b) active substances which have been classified in accordance with Regulation (EC) No 1272/2008 as mutagen category 1A or 1B; (c) active substances…

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

Evaluation of the Cosmetic Products Regulationfiled 12 Mar 2025PDFsource

COMMENTS OF THE CZECH REPUBLIC ON TARGETED REVISION OF THE COSMETIC PRODUCT REGULATION AND APPLICATION OF ARTICLE 15.2. ON NATURAL COMPLEX SUBSTANCES (NCSS) The Czech Republic for the area of cosmetic products provides an updated position on the targeted revision of the Cosmetic Product Regulation (CPR) and on the application of the article 15.2.

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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.

Showing 5 of 11.

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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.