Gaois

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2 results

  1. SOCIAL QUESTIONS|health|pharmaceutical industry · PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|intellectual property · PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research

    #675209

    IATE #799937
    deimhniú forlíontach cosanta le haghaidh táirgí íocshláinte Reference Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Context '... ciallaíonn ‘údarú margaíochta le haghaidh úsáid phéidiatraiceach’ údarú margaíochta a dheonaítear i leith táirge íocshláinte lena úsáid ag an duine nach gcosnaítear le deimhniú forlíontach cosanta faoi Rialachán (CE) Uimh. 469/2009 ó Pharlaimint na hEorpa agus ón gComhairle maidir leis an deimhniú forlíontach cosanta le haghaidh táirgí íocshláinte 65...' Reference "Togra le haghaidh Rialachán lena leagtar síos nósanna imeachta Aontais maidir le húdarú agus maoirseacht táirgí íocshláinte lena n-úsáid ag an duine agus lena mbunaítear rialacha lena rialaítear an Ghníomhaireacht Leigheasra Eorpach, lena leasaítear Rialachán (CE) Uimh. 1394/2007 agus Rialachán (AE) Uimh. 536/2014 agus lena n-aisghairtear Rialachán (CE) Uimh. 726/2004, Rialachán (CE) Uimh. 141/2000 agus Rialachán (CE) Uimh. 1901/2006, CELEX:52023PC0193/GA"
    ergänzendes Schutzzertifikat für Arzneimittel
    de
    supplementary protection certificate for medicinal products | SPC | SPCs | SPC for medicinal products
    en
    Definition certificate extending the duration of the intellectual property right in respect of a medicinal product covered by Regulation (EC) No 469/2009 Reference "Council-EN, based on definition on IATE:1268236 (""supplementary protection certificate"") and Regulation (EC) No 469/2009, CELEX:32009R0469/EN"
    Comment "The certificate is based on a patent covering the ""medicinal product"", which must have fallen within the scope of Regulation (EC) No 469/2009, CELEX:32009R0469/EN The duration of the intellectual property right may be extended by a maximum of 5 years (5.5 years in some cases). See also: supplementary protection certificate for plant protection products IATE:3533863<><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><><>"
    certificat complémentaire de protection pour les médicaments
    fr
    Definition titre de propriété industrielle créé par le règlement (CEE) nº1768/92 (tel que modifié depuis), qui permet de prolonger la protection d'un médicament soumis à autorisation de mise sur le marché et protégé par un brevet sur le territoire d'un État membre Reference Conseil-FR, d'après règlement (CE) nº469/2009 concernant le certificat complémentaire de protection pour les médicaments
    Comment "Il s'agit d'enrayer le recul de l'industrie pharmaceutique européenne sur le marché mondial face à la concurrence américaine et japonaise.Voir aussi:- IATE:1268236 certificat complémentaire de protection- IATE:3533863 certificat complémentaire de protection pour les produits phytopharmaceutiques."
  2. EUROPEAN UNION|European Union law|EU act · SOCIAL QUESTIONS|health|pharmaceutical industry · AGRICULTURE, FORESTRY AND FISHERIES|means of agricultural production|means of agricultural production · PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|intellectual property

    #656884

    IATE #3570854
    an Rialachán maidir le deimhnithe forlíontacha cosanta Reference Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Rialachán (CE) Uimh. 469/2009 maidir leis an deimhniú forlíontach cosanta le haghaidh táirgí íocshláinte Reference "Rialachán (CE) Uimh. 469/2009 maidir leis an deimhniú forlíontach cosanta le haghaidh táirgí íocshláinte, CELEX:32009R0469/GA ;Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    Verordnung (EG) Nr. 469/2009 über das ergänzende Schutzzertifikat für Arzneimittel | ESZ-Verordnung
    de
    SPC Regulation | EU SPC Regulation | Regulation on Supplementary Protection Certificates | Regulation (EC) No 469/2009 concerning the supplementary protection certificate for medicinal products
    en
    Comment Entry into force: 6.7.2009
    règlement CCP | règlement relatif au certificat complémentaire de protection | règlement (CE) n° 469/2009 concernant le certificat complémentaire de protection pour les médicaments
    fr