Gaois

Téarmaí cosúla:

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 »

35 toradh

  1. ENVIRONMENT|environmental policy|climate change policy · ENVIRONMENT|environmental policy

    #668983

    IATE #3639260
    deis thrialach rialála teicneolaíochta glan-nialasachta Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Leis na tionscadail straitéiseacha ghlan-nialasachta agus leis na deiseanna trialacha rialála teicneolaíochta glan-nialasachta, cuireadh i bhfeidhm na sásraí is gá chun iomaíochas fadtéarmach agus cumas nuálaíochta thionscal na hEorpa a áirithiú trí chumais mhonaraíochta, timpeallachtaí píolótacha le haghaidh tástála agus turgnamhaíochta, forálacha maidir le hacmhainneacht stórála CO2, an riosca a bhaint d’infheistíochtaí i dtionscadail straitéiseacha, chomh maith le gnólachtaí nuathionscanta, gnólachtaí atá i mbun fáis agus FBManna.' Tagairt "Togra le haghaidh Rialachán maidir le creat beart a bhunú chun éiceachóras monaraíochta teicneolaíochta glan-nialasachta na hEorpa a neartú (An Gníomh um an Tionscal Glan-nialasachta), CELEX:52023PC0161/GA"
    Sainmhíniú scéim lena gcuirtear ar a gcumas do ghnóthais teicneolaíochtaí glan-nialasachta nuálacha a thástáil i bhfíorthimpeallacht rialaithe, faoi phlean sonrach, a dhéanann údarás inniúil í a fhorbairt agus faireachán uirthi Tagairt "Togra le haghaidh Rialachán maidir le creat beart a bhunú chun éiceachóras monaraíochta teicneolaíochta glan-nialasachta na hEorpa a neartú (An Gníomh um an Tionscal Glan-nialasachta), CELEX:52023PC0161/GA"
    Nóta <<<_not_supplied_>>>
    Reallabor für Netto-Null-Technologien
    de
    Sainmhíniú Programm, das Unternehmen ermöglicht, innovative Netto-Null-Technologien in einem kontrollierten realen Umfeld im Rahmen eines spezifischen Plans zu testen, der von einer zuständigen Behörde entwickelt und überwacht wird Tagairt "Vorschlag für eine RICHTLINIE DES EUROPÄISCHEN PARLAMENTS UND DES RATES über den Führerschein, zur Änderung der Richtlinie (EU) 2022/2561 des Europäischen Parlaments und des Rates, der Verordnung (EU) 2018/1724 des Europäischen Parlaments und des Rates und zur Aufhebung der Richtlinie 2006/126/EG des Europäischen Parlaments und des Rates und der Verordnung (EU) Nr. 383/2012 der Kommission"
    net-zero regulatory sandbox
    en
    Sainmhíniú "scheme that enables undertakings to test innovative net-zero technologies in a controlled real-world environment, under a specific plan, developed and monitored by a competent authority" Tagairt "Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on establishing a framework of measures for strengthening Europe’s net-zero technology products manufacturing ecosystem (Net Zero Industry Act)"
    bac à sable réglementaire pour les technologies «zéro net»
    fr
    Nóta "Voir bac à sable réglementaire et technologie «zéro net»"
  3. INTERNATIONAL RELATIONS|defence · INTERNATIONAL ORGANISATIONS|world organisations|world organisation · ENERGY|electrical and nuclear industries|nuclear energy

    #613838

    IATE #912362
    CTBTO Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Eagraíocht an Chonartha um Chosc Cuimsitheach ar Thrialacha Núicléacha Tagairt "An tAcht um Chosc ar Thrialacha Núicléacha, 2008, http://www.acts.ie/ga.act.2008.0016.2.html [26.10.2018] ;Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    Organisation des Vertrags über das umfassende Verbot von Nuklearversuchen | CTBTO
    de
    Sainmhíniú zur Umsetzung des Vertrags über das umfassende Verbot von Nuklearversuchen gegründete Organisation mit Sitz in Wien, die bis zum Inkrafttreten des Vertrages auf provisorischer Basis arbeitet Tagairt "Council-DE gestützt auf Auswärtiges Amt, Vertrag über das umfassende Verbot von Atomtests https://www.auswaertiges-amt.de/de/aussenpolitik/themen/abruestung-ruestungskontrolle/nukleareabruestung/ctbt-node#content_0 (2.8.18)"
    Nóta "XREF: Vertrag über das umfassende Verbot von Nuklearversuchen IATE:882893 ; CTBTO-Vorbereitungskommission IATE:931543"
    Comprehensive Nuclear-Test-Ban Treaty Organization | CTBT Organization | CTBTO
    en
    Sainmhíniú "body to be established after entry into force of the CTBT [ IATE:882893 ]" Tagairt "CTBTO Preparatory Commission > Glossary > Comprehensive Nuclear-Test-Ban Treaty Organization, http://www.ctbto.org/index.php?id=280&no_cache=1&letter=c#comprehensive-nuclear-test-ban-treaty-organization- [4.8.2016]"
    Nóta "This body does not yet exist - see Preparatory Commission for the Comprehensive Nuclear-Test-Ban Treaty Organization [ IATE:931543 ]."
    Organisation du Traité d'interdiction complète des essais nucléaires | organisation du TICE | OTICE
    fr
    Sainmhíniú organisation qui n'existe pas encore mais qui devra être opérationnelle au moment de l'entrée en vigueur du traité d'interdiction complète des essais nucléaires et qui sera chargée d'assurer l'application des dispositions du traité et de ménager un cadre de consultation et de coopération Tagairt "Conseil-FR, d'après le site des Nations unies, ""Le Traité d'interdiction complète des essais nucléaires (TICE)"", http://www.un.org/fr/events/againstnucleartestsday/treaty.shtml [9.10.2017]"
    Nóta "À l'entrée en vigueur du Traité, cette organisation remplacera la Commission préparatoire de l'Organisation du Traité d'interdiction complète des essais nucléaires [IATE:931543 ].Voir aussi: - traité d'interdiction complète des essais nucléaires [IATE:882893 ]- Commission préparatoire de l'Organisation du Traité d'interdiction complète des essais nucléaires [IATE:931543 ]"
  4. TRANSPORT · TRANSPORT|land transport|land transport

    #553862

    IATE #1346481
    eitilt thrialach Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Prüfflug
    de
    check flight
    en
    Sainmhíniú a) a flight made to check or test the performance of an aircraft, rocket, or spacecraft, or a piece of equipment or component, or to obtain measurements or other data on performance; b) a familiarisation flight in an aircraft, or a flight in which a pilot or other aircrew member or members are tested or examined for proficiency Tagairt Multilingual Aeronautical Dictionary(AGARD,1980)
    vol de contrôle
    fr
  7. TRADE|marketing|preparation for market

    #551055

    IATE #1239260
    fochomhardú trialach Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Saldenliste
    de
    Sainmhíniú Liste mit den Salden, gegebenfalls mit den Soll-und Habenverkehrszahlen, derjenigen Konten, für die in der Bilanz ein Sammelkonto erscheint Tagairt International Accounting Lexicon(U.E.C.)-Konzernrechnungslegung
    subsidiary trial balance
    en
    Sainmhíniú a list of the balances on accounts,usually of debtors and creditors,for which a control account is kept Tagairt Internat.Account.Lex.,UEC-Group Accounts
    balance des comptes particuliers
    fr
    Sainmhíniú relevé des soldes éventuellement accompagnés des débits et crédits des comptes particuliers correspondant à un compte collectif Tagairt Internat.Accounting Lex.,UEC-Comptes de groupe
  9. PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research · ENERGY|electrical and nuclear industries|nuclear energy

    #605726

    IATE #778729
    Imoibreoir Trialach Teirmeanúicléach Idirnáisiúnta Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Beidh uasmhéid EUR 2,707 milliún (i bpraghsanna 2011) ar fáil don tionscadal d'Imoibreoir Trialach Teirmeanúicléach Idirnáisiúnta (ITTI) ó bhuiséad ginearálta an Aontais don tréimhse 2014 go 2020.' Tagairt " Rialachán ón gComhairle (AE, Euratom) Uimh. 1311/2013 lena leagtar síos an creat airgeadais ilbhliantúil do na blianta 2014 go 2020"
    ITER Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Más gá agus má tá bonn cirt cuí leis, féadfar leithreasaí a iontráil i mbuiséad Fís 2020 i ndiaidh 2020 d'fhonn costais cúnaimh riaracháin agus theicniúil a chumhdach, ionas go mbeifear in ann na gníomhaíochtaí nach mbeidh curtha i gcrích faoin 31 Nollaig 2020 a bhainistiú. Ní mhaoineofar le Fís 2020 tógáil nó oibriú clár Galileo, clár Copernicus nó an Comhghnóthas Eorpach d'ITER.' Tagairt "Rialachán (AE) Uimh. 1291/2013 ó Pharlaimint na hEorpa agus ón gComhairle lena mbunaítear Fís 2020 – An Clár Réime um Thaighde agus Nuálaíocht (2014-2020)"
    Internationaler Thermonuklearer Versuchsreaktor | ITER
    de
    Sainmhíniú gemeinsames Forschungsprojekt von EU und Japan, Kanada, Schweiz, Russland, VR China, Südkorea und USA, das Wege zu einer wirtschaftlichen Nutzung der kontrollierten Kernfusion aufzeigen soll Tagairt "http://de.wikipedia.org/wiki/ITER"
    Nóta "Standort des Versuchsreaktors: Cadarache (Südfrankreich); XREF: ITER-Organisation IATE:2225041 , ITER-Übereinkommen IATE:2232426 ; DIV: hm, 15.2.2006; UPD:aih, 12.1.07"
    international thermonuclear experimental reactor | ITER
    en
    Sainmhíniú ITER is an international tokamak (magnetic confinement fusion) research project designed to demonstrate the scientific and technological feasibility of a full-scale fusion power reactor. ITER is intended to be an experimental step between today's studies of plasma physics and future electricity-producing fusion power plants. It builds upon research conducted on devices such as DIII-D, EAST, TFTR, JET, JT-60, and T-15, and will be considerably larger than any of them. Tagairt "Wikipedia http://en.wikipedia.org/wiki/ITER (17.01.2007)"
    Nóta ITER is designed to produce approximately 500 MW (500,000,000 watts) of fusion power sustained for up to 500 seconds (compared to JET's peak of 16 MW for less than a second). A future fusion power plant would generate about 3000-4000 MW of thermal power.
    réacteur thermonucléaire expérimental international | ITER
    fr
    Sainmhíniú projet international qui a pour objectif de démontrer la possibilité scientifique et technologique de la production d'énergie par la fusion des atomes Tagairt ---
    Nóta Le réacteur ITER sera implanté à Cadarache, France.
  10. SOCIAL QUESTIONS|health|pharmaceutical industry

    #657567

    IATE #3571928
    sainchomhad iarratais ar thrialacha cliniciúla Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    sainchomhad iarratais Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Trí na nósanna imeachta nua maidir le húdarú trialacha cliniciúla, ba cheart taobhú leis an méid Ballstát agus is féidir a áireamh. Dá bhrí sin, ar mhaithe leis na nósanna imeachta a shimpliú maidir le tíolacadh sainchomhaid iarratais i dtaca le húdarú do thriail chliniciúil, ba cheart go seachnófaí faisnéis atá mar an gcéanna den chuid is mó a chur isteach arís agus arís eile agus ina ionad sin ba cheart aon sainchomhad iarratais amháin a chur isteach chuig na Ballstáit uile lena mbaineann trí thairseach tíolactha iarratais. I bhfianaise go bhfuil an tábhacht chéanna do thaighde cliniciúil Eorpach ag baint le trialacha cliniciúla a dhéantar i mBallstát aonair, ba cheart go ndéanfaí an sainchomhad iarratais do na trialacha cliniciúla sin a chur isteach freisin tríd an tairseach aonair sin.' Tagairt "Rialachán (AE) Uimh. 536/2014 maidir le trialacha cliniciúla ar tháirgí íocshláinte lena n-úsáid ag an duine, agus lena n-aisghairtear Treoir 2001/20/CE, CELEX:32014R0536/GA"
    Antragsdossier für die klinische Prüfung | Antragsdossier
    de
    Sainmhíniú "Unterlagen, die der Sponsor den betroffenen Mitgliedstaaten seiner Wahl über das EU-Portal übermittelt, um eine Genehmigung für die Durchführung einer klinischen Prüfung zu erhalten" Tagairt "COM-DE nach: Verordnung (EU) Nr. 536/2014 des Europäischen Parlaments und des Rates vom 16. April 2014 über klinische Prüfungen mit Humanarzneimitteln und zur Aufhebung der Richtlinie 2001/20/EG Text von Bedeutung für den EWR"
    clinical trial application dossier | CTA dossier | application dossier | application dossier for the authorisation of a clinical trial
    en
    Sainmhíniú "collection of documents that must be submitted by the sponsor through the EU clinical trial portal to the intended Member States concerned in order to obtain an authorisation to conduct a clinical trial" Tagairt "COM-Terminology Coordination, based on: - Articles 5(1) and 80 of Regulation (EU) No 536/2014 on clinical trials on medicinal products for human use- European Medicines Agency. 'The EU clinical trial portal and database' (4.11.2020)"
  11. EUROPEAN UNION|EU institutions and European civil service|EU office or agency|European Medicines Agency · SOCIAL QUESTIONS|health|medical science|medical research

    #664288

    IATE #3591654
    tairseach trialacha cliniciúla an Aontais Eorpaigh Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    EU clinical trial portal
    en
    Sainmhíniú single entry point for submitting clinical trial information in the EU, which will be stored in the database Tagairt "European Medicines Agency. 'The EU clinical trial portal and database' (4.11.2020)"
    Nóta "The Board was updated on the quality and status of the ongoing development of the EU clinical trial portal and database, both of which are being carefully monitored. The Board heard that the development of the auditable release of the portal and database (release 0.7) is complete. The release is now in an intensive phase of pre-testing before formal user acceptance testing (UAT7) can start in early 2019. Taking into account the rate of progress with testing and bug fixing, and the relocation of the Agency, the audit field work will take place once the Agency has settled in Amsterdam, after March 2019. Dependent on successful completion of the audit and review by the Management Board around the end of 2019, the system could be ready to go live later in 2020."
  13. EUROPEAN UNION|European Union law|EU act · LAW|justice

    #653873

    IATE #3564844
    Treoir ó Pharlaimint na hEorpa agus ón gComhairle maidir le neartú ar ghnéithe áirithe de thoimhde na neamhchiontachta agus den cheart chun bheith i láthair le linn na trialach in imeachtaí coiriúla Tagairt "Rialachán (AE) 2023/1543 ó Pharlaimint na hEorpa agus ón gComhairle an 12 Iúil 2023 maidir le hOrduithe Eorpacha chun Fianaise a Thabhairt ar Aird agus Orduithe Caomhnaithe Eorpacha i gcomhair fianaise leictreonach in imeachtaí coiriúla agus chun pianbhreitheanna coimeádta a fhorghníomhú tar éis imeachtaí coiriúla"
    ga
    Richtlinie (EU) 2016/343 zur Stärkung bestimmter Aspekte der Unschuldsvermutung und des Rechts auf Anwesenheit in der Verhandlung in Strafverfahren
    de
    Directive (EU) 2016/343 on the strengthening of certain aspects of the presumption of innocence and of the right to be present at the trial in criminal proceedings | PDI | PDI Directive | PDI proposal | POI Directive
    en
    Sainmhíniú EU Directive aimed at strengthening certain aspects of the right of suspects or accused persons in criminal proceedings in the EU to be presumed innocent until proven guilty by a final judgment and to strengthen the right to be present at one's trial Tagairt "Council-EN, based on the Directive (EU) 2016/343 on the strengthening of certain aspects of the presumption of innocence and of the right to be present at the trial in criminal proceedings, CELEX:32016L0343/EN"
    Directive (UE) 2016/343 portant renforcement de certains aspects de la présomption d'innocence et du droit d'assister à son procès dans le cadre des procédures pénales
    fr
  14. SOCIAL QUESTIONS|health|medical science

    #640813

    IATE #2249704
    Uimhir Chaighdeánach Idirnáisiúnta um Thrialacha Rialaithe Randamaithe Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Internationale Standardnummer für kontrollierte klinische Studien
    de
    International Standard Randomised Controlled Trial Number | randomized clinical
    en
    Sainmhíniú simple numeric system for the unique identification of randomised controlled trials worldwide Tagairt "ISRCTN Register , http://isrctn.org/ [20.7.2009]"
    numérotation internationale standardisée des essais cliniques randomisés
    fr
    ISRCTN | IRSCTN
    mul
  15. SOCIAL QUESTIONS|health|pharmaceutical industry

    #634673

    IATE #1687928
    urraitheoir trialach cliniciúla Tagairt "Rialachán (AE) Uimh. 536/2014 maidir le trialacha cliniciúla ar tháirgí íocshláinte lena n-úsáid ag an duine, CELEX:32014R0536/GA Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    Comhthéacs 'Déanfaidh urraitheoir trialach cliniciúla a rinneadh i mBallstát amháin ar a laghad gach faisnéis ábhartha maidir leis na frithghníomhartha díobhálacha tromchúiseacha neamhthuartha amhrasta seo a leanas a thuairisciú go leictreonach agus gan mhoill don bhunachar sonraí leictreonach.' Tagairt "Rialachán (AE) Uimh. 536/2014 maidir le trialacha cliniciúla ar tháirgí íocshláinte lena n-úsáid ag an duine, CELEX:32014R0536/GA"
    urraitheoir Tagairt "Rialachán (AE) Uimh. 536/2014 maidir le trialacha cliniciúla ar tháirgí íocshláinte lena n-úsáid ag an duine, CELEX:32014R0536/GA Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    Comhthéacs 'Ba cheart a fhoráil sa nós imeachta um údarú gur féidir na hamlínte don mheasúnú a fhadú chun ligean don urraitheoir díriú ar cheisteanna nó barúlacha a ardaítear le linn an mheasúnaithe ar an sainchomhad iarratais. Thairis sin, ba cheart a áirithiú, laistigh den tréimhse fhadaithe, go bhfuil dóthain ama i gcónaí ann chun an fhaisnéis bhreise a cuireadh isteach a mheasúnú.' Tagairt "Rialachán (AE) Uimh. 536/2014 maidir le trialacha cliniciúla ar tháirgí íocshláinte lena n-úsáid ag an duine, CELEX:32014R0536/GA"
    Sainmhíniú duine aonair, cuideachta, institiúid nó eagraíocht a ghlacann freagracht as triail chliniciúil a thionscnamh agus a bhainistiú agus freisin as maoiniú trialach cliniciúla a chur ar bun Tagairt "Rialachán (AE) Uimh. 536/2014 maidir le trialacha cliniciúla ar tháirgí íocshláinte lena n-úsáid ag an duine, CELEX:32014R0536/GA"
    Sponsor
    de
    Sainmhíniú eine Person, ein Unternehmen, eine Einrichtung oder eine Organisation, die bzw. das die Verantwortung für die Einleitung, das Management und die Aufstellung der Finanzierung einer klinischen Prüfung übernimmt Tagairt "Verordnung (EU) Nr. 536/2014 des Europäischen Parlaments und des Rates vom 16. April 2014 über klinische Prüfungen mit Humanarzneimitteln und zur Aufhebung der Richtlinie 2001/20/EG CELEX:32014R0536/DE"
    sponsor | clinical trial sponsor
    en
    Sainmhíniú individual, company, institution or organisation which takes responsibility for the initiation, for the management and for setting up the financing of the clinical trial Tagairt "Regulation (EU) No 536/2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC, CELEX:32014R0536/EN"