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Modifica dei regolamenti (CE) n. 1272/2008, (CE) n. 1223/2009 e (UE) 2019/1009 per quanto riguarda la semplificazione di alcune prescrizioni e procedure per i prodotti chimici

Dimitris Tsiodras, Piotr Müller – Proposta di reiezione – Emendamento 119
Data: 22.10.2026·Riferimento: A10-0104/2026
Relatore: Piotr Müller, Dimitris Tsiodras

Risultato complessivo

Respinta
  • 93 A favore
  • 480 Contro
  • 2 Astensione
  • 145 Non ha votato
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Svolgimento della procedura

2025/0531(COD) · COD

Attività documentate della procedura. Non stabiliscono se una legge sia entrata in vigore.

  1. Documentato: Deferimento123 giorni alla fase successiva
  2. Documentato: Esame in commissione101 giorni alla fase successiva
  3. Documentato: Plenaria9 giorni alla fase successiva
  4. Documentato: Negoziati76 giorni alla fase successiva
  5. Documentato: Esame in commissione92 giorni alla fase successiva
  6. Ultimo documentato: Plenaria30 giorni dall’inizio di questa fase
Attività documentate (24)
  1. Deferimento alla commissione
  2. Relazione della commissione presentata
  3. Emendamenti presentati in commissione
  4. Emendamenti presentati in commissione
  5. Emendamenti presentati in commissione
  6. Parere della commissione approvato
  7. Emendamenti presentati in commissione
  8. Relazione della commissione approvata
  9. Presentazione in plenaria
  10. Testo emendato in plenaria
  11. Rinvio in commissione per negoziati interistituzionali
  12. Votazione in plenaria
  13. Risultati della votazione in plenaria
  14. Negoziati interistituzionali
  15. Accordo provvisorio approvato in commissione
  16. Presentazione in plenaria
  17. Presentazione in plenaria
  18. Presentazione in plenaria
  19. Presentazione in plenaria
  20. Presentazione in plenaria
  21. Posizione del Parlamento in prima lettura
  22. Discussione in plenaria
  23. Votazione in plenaria
  24. Risultati della votazione in plenaria
Attività previste (non confermano lo svolgimento)
  1. Votazione in plenaria
  2. Discussione in plenaria
  3. Votazione in plenaria

Scheda della procedura (OEIL) · Dati del Parlamento europeo
Consultato il:

Fonti

Dati: EP Open Data API

Di cosa si tratta?

  • Simplification of labeling rules for chemical products and fertilizers.
  • Introduction of digital contact details on labels to speed up controls.
  • Boosting competitiveness by simplifying procedures for SMEs.
Fonte: riassunto generato da IA con Mistral

Cronologia degli emendamenti (13)

Testo come pubblicato dal PE, in inglese.

  1. Emendamento 90 · Proposta di reiezione della proposta della CommissioneRespinta

    Citation 5 a (new)

    Presentato da Per Clausen, Anja Hazekamp, Emma Fourreau · The Left

    Aggiunto: The European Parliament rejects the Commission proposal.

  2. Emendamento 91 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Recital 15 a (new)

    Presentato da Per Clausen, Anja Hazekamp, Emma Fourreau · The Left

    Aggiunto: (15a) In the Chemical Strategy for Sustainability, the Commission committed to ensure that consumer products, including cosmetics do not contain chemicals that cause cancers, gene mutations, affect the reproductive or the endocrine system, or are persistent and bioaccumulative.

  3. Emendamento 92 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Recital 15 b (new)

    Presentato da Per Clausen, Anja Hazekamp, Emma Fourreau · The Left

    Aggiunto: (15b) Endocrine disrupting chemicals are increasingly linked to diseases acting via the hormonal system. Their use represents a serious risk to human health as well as creating an economic cost for society. As hormones control brain development and growth, exposure to endocrine-disruptors during foetal development and puberty can lead to irreversible effects, some being detected only many years later. Endocrine-related disorders impact in particular the functioning of the thyroid, the immune system, the reproduction system and the overall human metabolism. Cosmetics should not contain endocrine disrupting chemicals.

  4. Emendamento 93 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Recital 22

    Presentato da Per Clausen, Anja Hazekamp, Emma Fourreau · The Left

    … and destroy the unsold products not complying with the new requirements. Therefore, Rimosso: periods of 12 months for placing and 24 Aggiunto: a period of 6 months for making available on the market of cosmetic products containing the …

  5. Emendamento 95 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Article 2 – paragraph 1 – point 2 – point a a (new)

    Presentato da Per Clausen, Anja Hazekamp, Emma Fourreau · The Left

    Aggiunto: (aa) The following paragraph is inserted after the second paragraph: 2a. The use in cosmetic products of substances classified as endocrine disruptor for human health of category 1A or 1B, or category 2 under Part 3 of Annex VI to Regulation (EC) No 1272/2008 shall be prohibited.

  6. Emendamento 96 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Article 2 – paragraph 1 – point 2 – point b

    Presentato da Per Clausen, Anja Hazekamp, Emma Fourreau · The Left

    Rimosso: Cosmetic products containing a substance classified as Aggiunto: Where a CMR substance of category 1A, 1B, or 2 Aggiunto: or an endocrine disruptor for human health of category 1 or 2, classified under Part 3 of Annex VI to Regulation (EC) No Rimosso: 1272/2008 prohibited from use in cosmetic products or such substance Aggiunto: 1272/2008, following a derogation request made in accordance with paragraph 1 or paragraph 2, second subparagraph, is prohibited or further restricted from use, cosmetic products containing that substance or not compliant with a restriction may continue to be Rimosso: placed on the market for 12 months and be made available on the market for Rimosso: 24 Aggiunto: 6 months after the entry into force of the relevant amendments to the …

  7. Emendamento 97 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Article 2 – paragraph 1 – point 2 – point b

    Presentato da Per Clausen, Anja Hazekamp, Emma Fourreau · The Left

    Aggiunto: The following paragraph is inserted after the seventh paragraph: Where cosmetic products containing a substance prohibited from use in cosmetic products or such substance not compliant with a restriction are placed or made available on the market during the set transition period, they shall bear a clear notice on the front of the packaging indicating the presence of the concerned substance and its classification, including the relevant signal word and hazard pictogram, ensuring that it is clear to the consumers that these substances pose risks to human health.

  8. Emendamento 98 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Recital 2 a (new)

    Presentato da Antonín Staněk, Mathilde Androuët, Valérie Deloge +6 · PfE

    Aggiunto: (2 a) Agricultural producers in the Union are increasingly exposed to international competition from third countries where regulatory, environmental and safety requirements are less stringent. This situation creates significant distortions of competition and places Union farmers at a disadvantage. In this context, it is essential that regulatory framework affecting fertilising products and agricultural inputs do not further increase production costs for Union farmers, while at the same time enhance their competitiveness, innovation and resilience.

  9. Emendamento 100 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Recital 22 a (new)

    Presentato da Marie Toussaint · Verts/ALE

    Aggiunto: (22 a) Per- and polyfluorinated alkyl substances (PFAS) are a large family of more than 10 000 man-made chemicals. PFAS have been used in an increasingly wide range of products, including cosmetic products. A core concern is the persistency of all PFAS leading to increasing environmental concentrations. Moreover, exposure to the most studied PFAS has been associated with a range of adverse health effects. The use of PFAS in cosmetics and its ingredients should be prohibited.

  10. Emendamento 101 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Article 2 – paragraph 1 – point 2 a (new)

    Presentato da Marie Toussaint · Verts/ALE

    Aggiunto: (2 a) The following Article is inserted: Article 15a Per- and polyfluoroalkyl substances (PFAS) 1. The intentional use of per- and polyfluoroalkyl substances (PFAS) shall be prohibited in cosmetic products. ‘PFAS’ means any substance that contains at least one fully fluorinated methyl (CF3 -) or methylene (-CF2 -) carbon atom (without any H/Cl/Br/I attached to it. 2. Paragraph 1 shall apply as of [OP: please insert the date of 18 months after entry into force of this Regulation]. 3. Restrictions or prohibitions on the use of PFAS laid down in accordance with Regulation (EC) No 1907/2006 or (EU) 2019/1021 of the European Parliament and of the Council shall take precedence over paragraph 1.

  11. Emendamento 104 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Article 2 – paragraph 1 – point 2 – point -a (new)

    Presentato da Marie Toussaint · Verts/ALE

    Rimosso: The Aggiunto: (-a) paragraph 1 is replaced by the following "The use in cosmetic products of substances classified as CMR Rimosso: substances, Aggiunto: substances of category 1A or 1B Aggiunto: and of endocrine disruptors of category 1 under Part 3 of Annex VI to Regulation (EC) No 1272/2008 shall be Rimosso: prohibited. Aggiunto: prohibited." (in case of adoption, Article 13(1), the title of Article 15, Article 15(2) second subparagraph and subparagraph 4a, Article 15(7) and Recital 22 should be modified accordingly)

  12. Emendamento 105 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Article 2 – paragraph 1 – point 2 – point b

    Presentato da Marie Toussaint · Verts/ALE

    Aggiunto: Cosmetic products containing a substance classified as a CMR substance of category 1A, 1B, or 2 under Part 3 of Annex VI to Regulation (EC) No 1272/2008 prohibited from use in cosmetic products and for which no derogation request was submitted in accordance with paragraph 2 or such substance is not compliant with a restriction may continue to be made available on the market until three months after the entry into force of the relevant amendments to the relevant Annexes to this Regulation. Cosmetic products containing a substance classified as a CMR substance of category 1A, 1B, or 2 under Part 3 of Annex VI to Regulation (EC) No 1272/2008 prohibited from use in cosmetic products and for which a derogation request was submitted in accordance with paragraph 2, but not granted due to safety concerns by the SCCS or such substance not compliant with a restriction may continue to be made available on the market until three months after the entry into force of the relevant amendments to the relevant Annexes to this Regulation. Cosmetic products containing a substance classified as a CMR substance of category … use in cosmetic products or such substance not compliant with a restriction Aggiunto: and for which a derogation request was submitted in accordance with paragraph 2 of this Article, but not granted due to the availability of a suitable alternative, may continue to Rimosso: be placed on the market for 12 months and be made available on the market for 24 months after the entry into force of the relevant amendments to the relevant Annexes to this Rimosso: Regulation.’ Aggiunto: Regulation and where an updated cosmetic product safety report (CPSR) remains available, where needed.' (Amendment further away from the COM proposal as compared to AM 61 by deleting any delays for “placing on the market”, and by reducing the delays for making available on the market in the first two cases to three months as compared to fifteen or twelve months, outweighing not changing the delay of 24 months for the third case)

  13. Emendamento 117 · Modifiche al regolamento (CE) n. 1223/2009Respinta

    Article 2 – paragraph 1 – point 2 – point a – point i a (new)

    Presentato da Sigrid Friis, Christel Schaldemose, Yvan Verougstraete +58 · Members

    Aggiunto: (i a) The first subparagraph is replaced by the following: 2. The use in cosmetic products of substances classified as CMR substances, of category 1A or 1B, or as endocrine disruptors for human health, of category 1 or 2, under Part 3 of Annex VI to Regulation (EC) No 1272/2008 shall be prohibited.

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