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Baza informacij za delovanje Partnerjev Mreže Modro Poslovanje

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CELEX:62024TJ0444:           Arrêt du Tribunal (sixième chambre) du 10 septembre 2025.#Montres Tudor SA contre Office de l’Union européenne pour la propriété intellectuelle.#Marque de l’Union européenne – Enregistrement international désignant l’Union européenne – Marque verbale 1926 – Motif absolu de refus – Caractère descriptif – Absence de caractère distinctif – Article 7, paragraphe 1, sous b) et c), du règlement (UE) 2017/1001.#Affaire T-444/24.

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CELEX:62024TJ0448: Judgment of the General Court (Third Chamber) of 10 September 2025.#JSherwood sp. z o.o. v European Union Intellectual Property Office.#EU trade mark – Opposition proceedings – Application for EU figurative mark JSherWood wear it with pride – Earlier EU word marks SHER-WOOD and SHER-WOOD SL and earlier EU figurative mark SHERWOOD – Relative ground for refusal – Likelihood of confusion – Similarity between products – Article 8(1)(b) of Regulation (EU) 2017/1001.#Case T-448/24.

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CELEX:62024TJ0448_INF: Judgment of the General Court (Third Chamber) of 10 September 2025.#JSherwood sp. z o.o. v European Union Intellectual Property Office.#EU trade mark – Opposition proceedings – Application for EU figurative mark JSherWood wear it with pride – Earlier EU word marks SHER-WOOD and SHER-WOOD SL and earlier EU figurative mark SHERWOOD – Relative ground for refusal – Likelihood of confusion – Similarity between products – Article 8(1)(b) of Regulation (EU) 2017/1001.#Case T-448/24.

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CELEX:62024TJ0449: Judgment of the General Court (First Chamber) of 30 September 2026.#Dryade VZW and Others v European Commission.#Environment – Aarhus Convention – Rejection of a request for internal review – Article 10(1) of Regulation (EC) No 1367/2006 – Delegated Regulation (EU) 2023/2485 – Maritime and aviation sectors – Taxonomy – Requirements for technical screening criteria – Article 19 of Regulation (EU) 2020/852 – Precautionary principle – Error of law – Manifest error of assessment.#Case T-449/24.

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CELEX:62024TJ0455: Judgment of the General Court (Fifth Chamber) of 23 September 2026 (Extracts).#Advanz Pharma Ltd v European Commission.#Public health – Medicinal products for human use – Orphan medicinal product for human use Ocaliva – obeticholic acid – Revocation of the conditional marketing authorisation – Procedure for review – Procedure initiated without awaiting the outcome of the renewal procedure – Consultation of an ad-hoc expert group by the EMA’s Committee for Medicinal Products for Human Use – Impartiality of the experts consulted – Declaration of a conflict of interest – Procedural defect – Principle of sound administration – Article 116 of Directive 2001/83/EC, as amended by Directive 2004/27/EC – Manifest errors of assessment – Legitimate expectations – Proportionality –

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CELEX:62024TJ0455_EXT: Judgment of the General Court (Fifth Chamber) of 23 September 2026 (Extracts).#Advanz Pharma Ltd v European Commission.#Public health – Medicinal products for human use – Orphan medicinal product for human use Ocaliva – obeticholic acid – Revocation of the conditional marketing authorisation – Procedure for review – Procedure initiated without awaiting the outcome of the renewal procedure – Consultation of an ad-hoc expert group by the EMA’s Committee for Medicinal Products for Human Use – Impartiality of the experts consulted – Declaration of a conflict of interest – Procedural defect – Principle of sound administration – Article 116 of Directive 2001/83/EC, as amended by Directive 2004/27/EC – Manifest errors of assessment – Legitimate expectations – Proportionalit

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CELEX:62024TJ0455_RES: Judgment of the General Court (Fifth Chamber) of 23 September 2026 (Extracts).#Advanz Pharma Ltd v European Commission.#Public health – Medicinal products for human use – Orphan medicinal product for human use Ocaliva – obeticholic acid – Revocation of the conditional marketing authorisation – Procedure for review – Procedure initiated without awaiting the outcome of the renewal procedure – Consultation of an ad-hoc expert group by the EMA’s Committee for Medicinal Products for Human Use – Impartiality of the experts consulted – Declaration of a conflict of interest – Procedural defect – Principle of sound administration – Article 116 of Directive 2001/83/EC, as amended by Directive 2004/27/EC – Manifest errors of assessment – Legitimate expectations – Proportionalit

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