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- Bylos, kuriose viena iš šalių yra ECHA
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Bylos, kuriose ECHA yra atsakovė arba į bylą įstojusi šalis
Bylos, kuriose ECHA yra atsakovė arba į bylą įstojusi šalis
Bylos, kuriose ECHA yra atsakovė arba į bylą įstojusi šalis
Šioje lentelėje išvardytos visos užbaigtos teismo bylos su nuosprendžiais, kuriose ECHA yra viena iš šalių. Suinteresuotosios šalys gali lengvai rasti joms aktualius sprendimus, susijusius su pagrindinėmis ECHA veiklos sritimis (REACH, CLP ir kt.) Kai kuriose bylose sprendimas dar nepriimtas laukiant apeliacijos nagrinėjimo rezultatų arba kito teismo sprendimo. Tai taip pat nurodyta lentelėje. Lentelėje nepateiktos su darbuotojais ar viešaisiais pirkimais susijusios bylos.
Užbaigtos teismo bylos suskirstytos į aštuonias kategorijas:
- REACH kandidatinis sąrašas: su labai didelį susirūpinimą keliančių cheminių medžiagų nustatymu susijusios bylos;
- REACH registracija: bylos, susijusios su bendro duomenų teikimo prievole;
- REACH autorizacija: su cheminės medžiagos įtraukimu į autorizacijos sąrašą (XIV priedas) ir paraiškomis autorizacijai gauti susijusios bylos;
- REACH vertinimas: bylos, kai vykstant vertinimo procedūrai (pagal REACH reglamento 40, 41 ar 46 straipsnius) ECHA paprašė registruotojo pateikti daugiau informacijos;
- suderinta klasifikacija: su cheminės medžiagos suderinta klasifikacija susijusios bylos;
- biocidai: su biocidais susijusios bylos;
- susipažinimas su dokumentais: su prašymais susipažinti su dokumentais susijusios bylos;
- įmonės dydis: su įmonių dydžio patikra ir atitinkamų mokesčių mokėjimu susijusios bylos.
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 |