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Cóip statach de shonraí a easpórtáiltear ó IATE ó am go chéile atá sa chnuasach seo. Níor cheart glacadh leis gurb ionann i gcónaí an t-eolas a thugtar faoi iontráil anseo agus a bhfuil sa leagan reatha den iontráil ar IATE. Is féidir an leagan reatha sin a cheadú ach cliceáil ar an nasc atá ar thaobh na láimhe deise ag barr gach iontrála. Breis eolais »

2 thoradh

  1. TRANSPORT|land transport|land transport|road transport

    #666194

    IATE #3620440
    lárchóras teannaidh bonn Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    central tyre inflation system | CTIS
    en
    Sainmhíniú a system fitted on a vehicle which controls the air pressure in each tyre fitted to an axle of the vehicle with air pressure from a vehicle mounted reservoir (infrastructure) while the vehicle is running but not limited to Tagairt "UN Regulation No 141 – Uniform provisions concerning the approval of vehicles with regard to their Tyre Pressure Monitoring Systems (TPMS) (2021/1463)"
  2. SOCIAL QUESTIONS|health|pharmaceutical industry · EUROPEAN UNION|EU institutions and European civil service|EU office or agency|European Medicines Agency · PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research|scientific research

    #666540

    IATE #3623655
    an Córas Faisnéise maidir le Trialacha Cliniciúla Tagairt "Rialachán Cur Chun Feidhme (AE) 2022/20 lena leagtar síos rialacha maidir le cur i bhfeidhm Rialachán (AE) Uimh. 536/2014 ó Pharlaimint na hEorpa agus ón gComhairle a mhéid a bhaineann le bunú na rialacha agus na nósanna imeachta um chomhar idir na Ballstáit sa mheasúnú sábháilteachta ar thrialacha cliniciúla, CELEX:32022R0020/GA Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    CTIS Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Informationssystem für klinische Prüfungen | CTIS
    de
    Sainmhíniú "System, das von der Europäischen Arzneimittel-Agentur in Zusammenarbeit mit den Mitgliedstaaten und der Europäischen Kommission eingerichtet und gepflegt wird und das zentrale EU-Portal sowie die EU-Datenbank für klinische Prüfungen enthält, die gemäß der Verordnung (EU) Nr. 536/2014 erforderlich sind" Tagairt "COM-DE nach:European Medicines Agency > Human regulatory > Research and development > Clinical trials > Clinical Trials Regulation (22.12.2021)"
    Clinical Trials Information System | CTIS
    en
    Sainmhíniú system set up and maintained by the European Medicines Agency, in collaboration with the Member States and the European Commission, which contains the centralised EU portal and database for clinical trials provided for in Regulation (EU) No 536/2014 Tagairt "COM-Terminology Coordination, based on: EMA (European Medicines Agency). 'Clinical Trials Regulation' (8.12.2021)"
    Nóta EU portal (Article 80) and database (Article 81) for clinical trials provided for in Regulation (EU) No 536/2014