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3 results in 3 documents

  1. #2375819

    Ullmhú le haghaidh cur chun feidhme na Comhdhála Idirnáisiúnta um Chomhchuibhiú Ceanglas Teicniúil i ndáil le Clárú Cógaisíochta atá le hÚsáid ag an Duine (ICH), i gcreat an chomhfhogasaithe le acquis cógaisíochta AE.

    Prepare for the implementation of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), in the framework of approximation with the EU pharma acquis.

    Recommendation No 1/2022 of the EU-Georgia Association Council of 16 August 2022 on the EU-Georgia Association Agenda 2021-2027 [2022/1422]

  2. #2383275

    Ullmhú le haghaidh threoirlínte na Comhairle Idirnáisiúnta um Chomhchuibhiú Ceanglas Teicniúil i ndáil le hEarraí Cógaisíochta atá le hÚsáid ag an Duine agus tosú ar a gcur chun feidhme.

    Prepare for and start implementing the guidelines of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH).

    Recommendation No 1/2022 of the EU-Republic of Moldova Association Council of 22 August 2022 on the EU-Republic of Moldova Association Agenda [2022/1997]

  3. #1951996

    Leis na caighdeáin ábhartha do na táirgí a chumhdaítear leis an Iarscríbhinn seo, áiritheofar ardleibhéal cosanta don tsláinte phoiblí ar aon dul leis na caighdeáin, na cleachtais agus na treoirlínte a d’fhorbair an Eagraíocht Dhomhanda Sláinte (EDS), an Eagraíocht um Chomhar agus Forbairt Eacnamaíochta (ECFE), an Chomhairle Idirnáisiúnta um Chomhchuibhiú Ceanglas Teicniúil um Chógaisíocht lena nÚsáid ag an Duine (ICH), agus an Comhar Idirnáisiúnta maidir le Comhchuibhiú Ceanglas Teicniúil do Chlárú Táirgí Íocshláinte Tréidliachta (VICH).

    The relevant standards for the products covered by this Annex shall ensure a high level of protection of public health in line with standards, practices and guidelines developed by the World Health Organization (WHO), the Organization for Economic Cooperation and Development (OECD), the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), and the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH).

    Trade and Cooperation Agreement between the European Union and the European Atomic Energy Community, of the one part, and the United Kingdom of Great Britain and Northern Ireland, of the other part