- ECHA
- O nama
- Način rada
- Postupci i politike
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- Predmeti u kojima ECHA nastupa kao stranka u postupku
- Biocides
Predmeti u kojima je ECHA tužena strana ili intervenijent
Predmeti u kojima je ECHA tužena strana ili intervenijent
Predmeti u kojima je ECHA tužena strana ili intervenijent
Sljedeća tablica sadrži sve sudske predmete okončane presudom u kojima je ECHA bila stranka u postupku. Zainteresirane strane jednostavno se mogu pozvati na odluke koje su za njih relevantne u sklopu osnovnih aktivnosti ECHA-e (uredbe REACH, CLP, i druge). Za neke je predmete u postupku žalba ili daljnje upućivanje odnosno uzvrat, što je također navedeno u tablici. U tablici nisu navedeni predmeti koji se bave osobljem ili javnom nabavom.
Riješeni sudski predmeti razvrstani su u osam kategorija:
- Popis predloženih tvari prema REACH-u: predmeti vezani uz identifikaciju posebno zabrinjavajućih tvari;
- Registracija u skladu s Uredbom REACH: predmeti povezani s obvezom zajedničkog podnošenja podataka;
- Autorizacija prema REACH-u: predmeti vezani uz uvrštavanje tvari u popis tvari koje podliježu autorizaciji (prilog XIV.) i uz zahtjeve za davanje autorizacije;
- Evaluacija prema REACH-u: predmeti u kojima je ECHA u okviru postupka evaluacije zatražila informacije od podnositelja registracije (članci 40., 41. ili 46. Uredbe REACH);
- CLH: predmeti koji se bave usklađivanjem razvrstavanja tvari;
- Biocidi: predmeti koji se odnose na biocide;
- ATD: predmeti vezani uz pristup dokumentima;
- Veličina poduzeća: predmeti vezani uz potvrđivanje veličine poduzeća i povezane naknade.
Case number | Parties | Keywords | Main Legal Provisions | Procedurally linked cases | Date of the ruling |
---|---|---|---|---|---|
T-669/15 R | Lysoform Dr. Hans Rosemann and Others v ECHA | Application for interim measures — REACH — Making available on the market and use of biocidal products — Inclusion of a company as a supplier of an active substance on the list referred to in Article 95 of Regulation (EU) No 528/2012 — Application for suspension of operation — Lack of urgency |
Art. 278, 279, 256(1) of TFEU; Art. 95 of BPR; Art. 7 of the Charter of Fundamental Rights |
Initial Case: Appeal on the Initial Case: |
17/12/2015 |
T-543/15R | Lysoform Dr. Hans Rosemann and Others v ECHA | Application for interim measures — REACH — Making available on the market and use of biocidal products — Inclusion of a company as a supplier of an active substance on the list referred to in Article 95 of Regulation (EU) No 528/2012 — Application for suspension of operation — Lack of urgency |
Art. 278, 279, 256(1) of TFEU; Art. 95 of BPR; Art. 7 of the Charter of Fundamental Rights |
Initial Case: Appeal on the Initial Case: |
17/12/2015 |
T-669/15 | Lysoform Dr. Hans Rosemann and Others v ECHA | Actions for annulment — Inclusion as supplier of an active substance on the list provided for in Article 95 of Regulation (EU) No 528/2012 — Lack of direct concern — Inadmissibility | Art. 95 of BPR; Art. 263 of TFEU |
|
12/10/2016 |
T-543/15 | Lysoform Dr. Hans Rosemann and Others v ECHA | Actions for annulment — Inclusion as supplier of an active substance on the list provided for in Article 95 of Regulation (EU) No 528/2012 — Lack of direct concern — Inadmissibility | Art. 95 of BPR; Art. 263 of TFEU |
|
12/10/2016 |
C-663/16 P | Lysoform Dr. Hans Rosemann and Ecolab Deutschland v ECHA | Appeal — Article 181 of the Rules of Procedure of the Court of Justice –– Regulation (EU) No 528/2012 — Making available on the market and use of biocidal products — Article 95 — European Chemicals Agency (ECHA) — Publication of a list of active substances — Inclusion of a company as a supplier of an active substance | Art. 130(1), 130(7) and 181 of the Rules of Procedure |
Initial Case: Proceedings for interim measures: |
19/07/2017 |
C-666/16 P | Lysoform Dr. Hans Rosemann and Ecolab Deutschland v ECHA | Appeal — Article 181 of the Rules of Procedure of the Court of Justice –– Regulation (EU) No 528/2012 — Making available on the market and use of biocidal products — Article 95 — European Chemicals Agency (ECHA) — Publication of a list of active substances — Inclusion of a company as a supplier of an active substance | Art. 130(1) and 130(7) of the Rules of Procedure |
Initial Case: Proceedings for Interim Measures: |
19/07/2017 |
T-243/17 | Ecolab Deutschland and Lysoform Dr. Hans Rosemann v ECHA | Removal from the register | Art. 263 of TFEU | 18/10/2017 | |
Laboratoire Pareva and Biotech3D v Commission | Biocidal products – Active substance PHMB (1415; 4.7) – Refusal of approval for product-types 1, 5 and 6 – Conditional approval for product-types 2 and 4 – Risks to human health and the environment – Regulation (EU) No 528/2012 – Article 6(7)(a) and (b) of Delegated Regulation (EU) No 1062/2014 – Harmonised classification of the active substance under Regulation (EC) No 1272/2008 – Prior consultation of the ECHA – Manifest error of assessment – Read-across – Right to be heard |
Regulation (EU) 528/2012, |
15/09/2021 | ||
Sumitomo Chemical and Tenka Best v Commission | Removal from the registrer | 18/12/2019 | |||
Laboratoire Pareva v Commission | Biocidal products – Active substance PHMB (1415; 4.7) – Refusal of approval for product-types 1, 5 and 6 – Conditional approval for product-types 2 and 4 – Risks to human health and the environment – Regulation (EU) No 528/2012 – Article 6(7)(a) and (b) of Delegated Regulation (EU) No 1062/2014 – Harmonised classification of the active substance under Regulation (EC) No 1272/2008 – Prior consultation of the ECHA – Manifest error of assessment – Read-across – Right to be heard |
Regulation (EU) 528/2012, |
15/09/2021 | ||
EurO3zon v ECHA | Suspension of evaluation active substance - BPR Regulation | 08/04/2023 | |||
Laboratoire PAREVA S.A.S. v Commission | Appeal – Biocidal products – Regulation (EU) No 528/2012 – Delegated Regulation (EU) No 1062/2014 – Active substance PHMB (1415; 4.7) – Refusal of approval as an existing active substance for use in biocidal products of product-types 1, 5 and 6 – Approval as an existing active substance for use in biocidal products of product-types 2 and 4 – Teratogenic effect – Human health risk assessment |
Appeal – Biocidal products – Regulation (EU) No 528/2012 – Delegated Regulation (EU) No 1062/2014 – Active substance PHMB (1415; 4.7) – Refusal of approval as an existing active substance for use in biocidal products of product-types 1, 5 and 6 – Approval as an existing active substance for use in biocidal products of product-types 2 and 4 – Teratogenic effect – Human health risk assessment |
Appeal of the Cases T-337/18 and T-347/18 |
10/11/2022 | |
Sciessent LLC v Commission | Biocidal products – Active substances – Silver zeolite and silver copper zeolite – Refusal of approval for product-types 2 and 7 – Article 4 and Article 19(1)(b) of Regulation (EU) No 528/2012 – Efficacy – Active substances for use in treated articles – Assessment of the efficacy of the treated articles themselves – Competence of the Commission – Principle of non-discrimination – Legal certainty – Legitimate expectations |
Articles 3(1)(I), 4(1), 19(1), 19(2), Annex II, Annex VI of Regulation (No 528/2012) |
COM Decision 2019/1973 |
16/11/2022 | |
Sciessent LLC v Commission | Biocidal products – Active substances – Silver zeolite and silver copper zeolite – Refusal of approval for product-types 2 and 7 – Article 4 and Article 19(1)(b) of Regulation (EU) No 528/2012 – Efficacy – Active substances for use in treated articles – Assessment of the efficacy of the treated articles themselves – Competence of the Commission – Principle of non-discrimination – Legal certainty – Legitimate expectations |
Articles 3(1)(I), 4(1), 19(1), 19(2), Annex II, Annex VI of Regulation (No 528/2012) |
COM Decision 2019/1960 |
16/11/2022 |