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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 »

66 toradh

  1. EUROPEAN UNION|European Union law|EU act · LAW|justice

    #587395

    IATE #3564844
    Treoir ó Pharlaimint na hEorpa agus ón gComhairle maidir le gnéithe áirithe de thoimhde na neamhchiontachta a neartú mar aon leis an gceart bheith i láthair ag an triail in imeachtaí coiriúla Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    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 Directive | POI Directive | PDI | PDI proposal
    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
  2. PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research · SOCIAL QUESTIONS|health|pharmaceutical industry

    #565158

    IATE #1686966
    tástáil dall dúbailte Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Doppelblindstudie | Doppel-Blindversuch | Doppelblindversuch
    de
    Sainmhíniú Versuch, bei dem nicht nur die Versuchsperson, sondern auch Arzt und Versuchshelfer ueber die Art der verabreichten Medikamente nicht aufgeklaert werden Tagairt Real-Lex. Med
    double-blind study | double-blind | double blind assay | double-blinded test | double-blind trial | double blind test | double blindfold test | double-blinding
    en
    Sainmhíniú type of clinical trial in which neither the participants nor the researchers know which participants are receiving the experimental treatment and which participants are receiving the control treatment Tagairt AIDSinfo > Education Materials > Glossary > Double-Blind Study, http://aidsinfo.nih.gov/education-materials/glossary/211/double-blind-study [18.12.2012]
    essai en double anonymat | épreuve à double insu | essai en double insu | double aveugle | essai à double insu | essai en double-aveugle | test doublement anonyme
    fr
    Sainmhíniú essai au cours duquel ni le patient ni l'équipe soignante ne savent quel produit est effectivement pris: les volontaires participant à un essai en double aveugle sont répartis au hasard dans différents groupes (l'un des groupes reçoit le médicament expérimental, un autre le placebo ou le même médicament expérimental mais à une autre dose, ou bien encore un traitement de référence) Tagairt Act Up-Paris,Gloss.sida,janvier 1998
  3. EUROPEAN UNION|EU institutions and European civil service|EU office or agency|European Medicines Agency · SOCIAL QUESTIONS|health|medical science|medical research

    #597920

    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.
  4. EUROPEAN UNION|European construction|European Union · SOCIAL QUESTIONS|health|medical science · SOCIAL QUESTIONS|health|pharmaceutical industry

    #572524

    IATE #3502438
    EudraCT Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Bunachar Sonraí AE maidir le Trialacha Cliniciúla Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    EudraCT | Datenbank über klinische Prüfungen der Europäischen Union
    de
    EU Database on Clinical Trials | European Union clinical trials database | European Clinical Trials Database | database of clinical trials | clinical trials database | EudraCT
    en
    Sainmhíniú the EU’s electronic database of clinical trials Tagairt 'Overview of EudraCT'; https://eudract.ema.europa.eu/help/Default.htm [ 18.12.2013 ]
    Nóta It contains information submitted by sponsors and informs users about ongoing clinical trials in all EU Member States and European Economic Area (EEA) countries, enabling an overview of multi-state trials.See also: clinical trial (related) [ IATE:1686971 ]
    base de données de l'UE sur les essais cliniques | EudraCT
    fr
  5. PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research · SOCIAL QUESTIONS|health|pharmaceutical industry

    #599213

    IATE #3599551
    clár oibre an Aontais Eorpaigh um thrialacha cliniciúla ilionaid Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    EU-Plattform für multizentrische klinische Prüfungen
    de
    EU platform for multi-centre clinical trials
    en
    Sainmhíniú flexible, well-resourced platform for multi-centre trials to bring together existing European clinical trial networks for therapeutics and vaccines, making clinical research faster, broader and more effective Tagairt COM-EN, based on:- European Commission > Press release > 15 June 2021, Brussels > Emerging stronger from the pandemic: acting on the early lessons learnt (30.9.2021)- European Commission > Questions and answers > 16 September 2021, Brussels > Questions and Answers: European Health Emergency preparedness and Response Authority – HERA (30.9.2021)- Communication from the Commission - Drawing the early lessons from the COVID-19 pandemic, COM(2021) 380
    plateforme de l’UE pour les essais cliniques multicentriques
    fr
  6. INTERNATIONAL RELATIONS|cooperation policy · PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research · SOCIAL QUESTIONS|health

    #542471

    IATE #929310
    EDCTP Tagairt Comhairle-GA
    ga
    an Chomhpháirtíocht maidir le Trialacha Cliniciúla idir Tíortha Eorpacha agus Tíortha i mBéal Forbartha Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Partnerschaft Europas und der Entwicklungsländer im Bereich klinischer Studien | Partnerschaft der europäischen Länder und Entwicklungsländer zur Durchführung klinischer Studien | EDCTP-Programm
    de
    Sainmhíniú Langzeit-Initiative der Europäischen Kommission mit dem Ziel, die Entwicklung neuer klinischer Instrumente und Behandlungen gegen HIV/AIDS, Malaria und Tuberkulose in den Entwicklungsländern (insbesondere den afrikanischen Ländern südlich der Sahara) voranzutreiben Tagairt European Commission > Research > Europäische Forschung in Aktion > HIV/AIDS http://ec.europa.eu/research/leaflets/aids/article_2879_de.html (2.07.12)
    Nóta Die Partnerschaft wurde als unabhängige Organisation in der Rechtsform einer Europäischen wirtschaftlichen Interessenvereinigung (EWIV) mit Sitz in Den Haag, Niederlande, geschaffen.
    Innovative Medicines Initiative Programme | European and Developing Countries Clinical Trials Partnership | EDCTP | IMI2
    en
    Sainmhíniú partnership between 14 EU countries, Switzerland and Norway, and 47 sub-Saharan African countries, which aims to reduce poverty by developing new clinical interventions to fight HIV/AIDS, malaria and tuberculosis in sub-Saharan Africa Tagairt Commission staff working document - Progress made on the Millennium Development Goals and key challenges for the road ahead accompanying the Communication from the Commission to the European Parliament, the Council, the European Economic and Social Committee and the Committee of the Regions - A twelve-point EU action plan in support of the Millennium Development Goals, http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=SEC:2010:0418:FIN:EN:PDF
    partenariat des pays européens et en développement sur les essais cliniques | EDCTP | partenariat Europe - Pays en développement pour les essais cliniques | programme EDCTP
    fr
    Sainmhíniú partenariat créé en 2003 entre 14 pays de l'UE, la Norvège et la Suisse et 47 pays d'Afrique subsaharienne pour lutter contre les trois principales maladies liées à la pauvreté (VIH/sida, malaria et tuberculose), pour mettre en oeuvre un programme de recherche sur le développement de nouveaux produits médicaux, microbicides et vaccins axé sur les essais cliniques de phases II et III et adapté aux besoins spécifiques des pays en développement Tagairt Conseil-FR, d'après le site officiel de l'EDCTP, http://www.edctp.org/L_organisation.761.0.html (2.7.2012) et celui de la Commission européenne, http://ec.europa.eu/research/health/infectious-diseases/poverty-diseases/gen-info_fr.html
  8. LAW · LAW|rights and freedoms

    #527276

    IATE #154547
    triail chothrom Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    triail chóir Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    faires Verfahren
    de
    fair trial
    en
    Nóta The idea of a fair trial is central to human rights doctrine, not only as a right in itself, but because without this one right, all others are at risk; if the state is unfairly advantaged in the trial process, it cannot be prevented in the courts from abusing all other tights. (Source: A Dictionary of Human Rights, David Robertson, 2004) The terms 'fair trial' and 'fair hearing' are often used as synonyms, especially in the field of human rights. However, strictly speaking, 'fair hearing' is narrower in meaning.
    procès équitable
    fr
  9. AGRICULTURE, FORESTRY AND FISHERIES · ENVIRONMENT · PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research · PRODUCTION, TECHNOLOGY AND RESEARCH|technology and technical regulations|technology · SOCIAL QUESTIONS|health|medical science

    #552061

    IATE #1255424
    triail allamuigh Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Bunaíodh triail allamuigh, macsamhlaithe i dtrí fhoraois feirme difriúla i gCo Luimnigh, in earrach 2008 chun táirgeacht bheacán oisreacha (Pleurotus ostreatus) agus síotácha (Lentinula edodes) de lomáin gearrtha ó thanaithe foraoise a mheasúnú. Ar gach feirm bhí an triail déanta suas de 720 lomán (is é 500 lomán an íos-mhéid a thabharfadh aisíoc tráchtála).' Tagairt 'Tuarascáil Bhliantúil Coford 2008', Coford, http://www.coford.ie/media/coford/content/publications/projectreports/annualreports/2008_ar_I.pdf [22.3.2016]
    Feldversuch | Freilandversuch
    de
    field experiment | field trial
    en
    Sainmhíniú scientific method to experimentally examine an intervention in the real world (or as many experimentalists like to say, naturally occurring environments) rather than in the laboratory Tagairt Wikipedia. Field experiment http://en.wikipedia.org/wiki/Field_experiment [9.3.2012]
    Nóta See also: - clinical field trial (narrower) [ IATE:3555178 ]
    essai au champ | essais au champ | essais en champ | expérience de terrain | essai en champ | expérience sur le terrain
    fr
    Sainmhíniú essai de culture en milieu naturel visant à observer le comportement d'une plante en conditions réelles Tagairt COM-FR, d’après «En quoi consiste un essai en plein champ ?», ministère de l'Écologie, du Développement durable et de l'Énergie, http://www.developpement-durable.gouv.fr/En-quoi-consiste-un-essai-en-plein,26342.html [4.7.2014]
    Nóta Les essais en champ apportent des informations complémentaires de celles obtenues à partir des modèles mathématiques ou des essais en milieu confiné et ils valident les hypothèses initiales. Plus globalement, ils s’inscrivent dans un processus d’acquisition de connaissances et contribuent à estimer le comportement de la plante soumise à des environnements divers et variables. (source: Pourquoi des essais en champ ?, INRA, http://www.inra.fr/la_science_et_vous/dossiers_scientifiques/ogm/pourquoi_des_essais_en_champ [12.6.2012])
  10. EDUCATION AND COMMUNICATIONS|communications · INDUSTRY|mechanical engineering|mechanical engineering · PRODUCTION, TECHNOLOGY AND RESEARCH

    #562678

    IATE #1605660
    tástáil allamuigh Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    praktische Erprobung | Betriebsprüfung | Einsatzerprobung | Betriebsversuch
    de
    field trial | field test
    en
    Sainmhíniú test carried out in the environment in which a product or device is to be used Tagairt "field test" Oxford Dictionary of English (3 ed.) Edited by Angus Stevenson. Oxford University Press, 2010. http://www.oxfordreference.com/view/10.1093/acref/9780199571123.001.0001/m_en_gb0294350?rskey=P2NL2Y&result=3&q=field test [8.4.2013]
    essai en conditions réelles | essai sur site
    fr
    Sainmhíniú essai de conformité ou essai de détermination effectué à l'endroit où l'entité est utilisée et pendant lequel les conditions existantes de fonctionnement, d'environnement, de maintenance et de mesure sont relevées Tagairt Commission Electrotechnique Internationale (CEI), glossaire http://www.electropedia.org/iev/iev.nsf/display?openform&ievref=191-14-05 [11.12.2013]
  11. SOCIAL QUESTIONS|health|medical science

    #571784

    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
    randomized clinical | International Standard Randomised Controlled Trial Number
    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
  12. SOCIAL QUESTIONS|health|pharmaceutical industry

    #582126

    IATE #3543174
    triail chliniciúil íseal-idirghabhála Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    klinische Prüfung mit geringfügiger Intervention
    de
    Sainmhíniú klinische Prüfung, die folgende Bedingungen erfüllt: a) Die Prüfpräparate sind zugelassen; b) die Prüfpräparate sollen dem Prüfplan der klinischen Prüfung zufolge gemäß der im betroffenen Mitgliedstaat geltenden Zulassung verwendet werden oder werden in einem der betroffenen Mitgliedstaaten als Standardbehandlung verwendet; c) die zusätzlichen diagnostischen oder Überwachungsverfahren stellen im Vergleich zur normalen klinischen Praxis in dem betroffenen Mitgliedstaat nur ein geringfügiges zusätzliches Risiko bzw. eine geringfügige zusätzliche Belastung für die Sicherheit der Probanden dar Tagairt COM-Internes Dokument SANCO-2012-80155-02-01
    low-intervention clinical trial
    en
    Sainmhíniú clinical trial [ IATE:1686971 ] which fulfils all of the following conditions:(a) the investigational medicinal products [ IATE:2146586 ] are authorised;(b) according to the protocol of the clinical trial, the investigational medicinal products are used in accordance with the terms of the marketing authorisation or their use is a standard treatment; and(c) the additional diagnostic or monitoring procedures do not pose more than minimal additional risk or burden to the safety of the subjects compared to normal clinical practice Tagairt COM-EN, based on:Point (3) of the second paragraph of Article 2 of the proposal for a Regulation on clinical trials on medicinal products for human use (COM(2012) 369 final), CELEX:52012PC0369/EN
    essai clinique à faible intervention
    fr
    Sainmhíniú essai clinique [ IATE:1686971 ] obéissant à l’ensemble des conditions suivantes:a) les médicaments expérimentaux sont autorisés;b) selon le protocole de l’étude clinique, les médicaments expérimentaux sont utilisés conformément aux conditions de l’autorisation de mise sur le marché ou leur utilisation constitue un traitement standard;c) les procédures supplémentaires de diagnostic ou de surveillance impliquent au plus un risque ou une contrainte supplémentaire minimale pour la sécurité des participants par rapport à la pratique clinique normale Tagairt COM-Document interne: SANCO-2012-80155-00-04Règlement relatif aux essais cliniques de médicaments à usage humain
  14. PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research · SOCIAL QUESTIONS|health|pharmaceutical industry

    #568980

    IATE #2146586
    táirge íocshláinte imscrúdaitheach Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Prüfpräparat
    de
    Sainmhíniú pharmazeutische Form eines Wirkstoffs oder Placebos, die in einer klinischen Prüfung getestet oder als Referenzsubstanz verwendet wird Tagairt Richtlinie 2001/20/EG des Europäischen Parlaments und des Rates vom 4. April 2001 zur Angleichung der Rechts- und Verwaltungsvorschriften der Mitgliedstaaten über die Anwendung der guten klinischen Praxis bei der Durchführung von klinischen Prüfungen mit Humanarzneimitteln CELEX:32001L0020/DE
    investigational medicinal product | investigational product | IMP | medicinal product for trial
    en
    Sainmhíniú medicinal product which is being tested or used as a reference, including as a placebo, in a clinical trial Tagairt Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC
    Nóta These do not include medicinal products used for background treatment, challenge agents, rescue medication, or medicinal products used to assess end-points in a clinical trial.
    médicament expérimental
    fr
    Sainmhíniú médicament expérimenté ou utilisé comme référence, y compris en tant que placebo, lors d'un essai clinique Tagairt Règlement (UE) n o 536/2014 relatif aux essais cliniques de médicaments à usage humain et abrogeant la directive 2001/20/CE
  15. SOCIAL QUESTIONS|health|medical science|medical research · SOCIAL QUESTIONS|health|pharmaceutical industry

    #596909

    IATE #3589336
    triail chliniciúil randamaithe oiriúnaitheach ilionaid Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    multizentrische adaptive randomisierte klinische Prüfung
    de
    multi-centre adaptive randomised clinical trial
    en
    Sainmhíniú clinical trial that is multi-centre, randomised and adaptive Tagairt COM-Terminology Coordination
    essai clinique multicentrique, adaptatif et randomisé | essai clinique multicentré, randomisé et adaptatif | essai clinique multicentre, randomisé et adaptatif
    fr
    Nóta Voir aussi:- essai clinique- multicentrique- randomisé- adaptatif
  16. SOCIAL QUESTIONS|health|pharmaceutical industry

    #575869

    IATE #3518689
    staidéar ilionaid Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Beidh an fhoirm iarratais líonta isteach go cuí le faisnéis faoi na rudaí seo a leanas: ... 1.8. na Ballstáit agus na tríú tíortha ina ndéanfar an t-imscrúdú cliniciúil mar chuid de staidéar ilionaid nó ilnáisiúnta a shainaithint tráth a dtíolactar an t-iarratas...' Tagairt Rialachán (AE) 2017/745 maidir le feistí leighis, lena leasaítear Treoir 2001/83/CE, Rialachán (CE) Uimh. 178/2002 agus Rialachán (CE) Uimh. 1223/2009 agus lena n-aisghairtear Treoir 90/385/CEE ón gComhairle agus Treoir 93/42/CEE ón gComhairle, CELEX:32017R0745/GA
    triail chliniciúil ilionaid Tagairt 'Tuarascáil Bhliantúil 2016,' an Bord Taighde Sláinte, https://www.hrb.ie/fileadmin/2._Plugin_related_files/Publications/2017_and_earlier_Pubs/An_Bord_Taighde_Slainte_Tuarascail_Bhliantuil_2016.pdf [3.11.2020] ;Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    multizentrische klinische Prüfung | multizentrische Studie
    de
    Sainmhíniú nach einem einzigen Prüfplan durchgeführte klinische Prüfung, die in mehr als einer Prüfstelle erfolgt und daher von mehr als einem Prüfer vorgenommen wird, wobei die Prüfstellen sich in einem einzigen Mitgliedstaat, in mehreren Mitgliedstaaten und/oder in Mitgliedstaaten und Drittländern befinden können Tagairt Richtlinie 2001/20/EG des Europäischen Parlaments und des Rates vom 4. April 2001 zur Angleichung der Rechts- und Verwaltungsvorschriften der Mitgliedstaaten über die Anwendung der guten klinischen Praxis bei der Durchführung von klinischen Prüfungen mit Humanarzneimitteln
    multi-centre clinical trial | multicenter study | multicenter trial | multi-centre trial | multi-centre study
    en
    Sainmhíniú clinical trial conducted according to a single protocol but at more than one site, and therefore, carried out by more than one investigator Tagairt COM-Terminology Coordination, based on: European Commission > 'Good Clinical Practice*): Directive 75/318/EEC as amended (July 1996)' (2.6.2020)
    Nóta According to Directive 2001/20/EC the trial sites may be located in a single Member State, in a number of Member States and/or in Member States and third countries
    essai clinique multicentrique
    fr
    Sainmhíniú essai clinique mené sur plusieurs sites par différents investigateurs mais selon un même protocole Tagairt COM-FR d'après:site de la Fondation Synergie Lyon Cancer, Glossaire > multicentrique (27.4.2020)
  17. PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research|scientific research · SOCIAL QUESTIONS|health|pharmaceutical industry

    #599887

    IATE #3623643
    triail chliniciúil ilnáisiúnta 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
    Sainmhíniú triail chliniciúil ar chuir an t-urraitheoir sainchomhad iarratais faoi bhráid níos mó ná Ballstát amháin ina leith trí thairseach an Aontas 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
    multinationale klinische Prüfung
    de
    Sainmhíniú klinische Prüfung, für die der Sponsor ein Antragsdossier an mehr als einen Mitgliedstaat über das EU-Portal übermittelt hat Tagairt COM-internes Dokument: SANTE-2021-81060 (klinische Prüfungen)
    multi-national clinical trial
    en
    Sainmhíniú clinical trial for which the sponsor submitted an application dossier to more than one Member State through the EU portal Tagairt Commission Implementing Regulation (EU) 2022/20 laying down rules for the application of Regulation (EU) No 536/2014 as regards setting up the rules and procedures for the cooperation of the Member States in safety assessment of clinical trials
  18. PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research policy · SOCIAL QUESTIONS|health|pharmaceutical industry

    #582182

    IATE #3543771
    tástáil oscailte Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    offene Studie
    de
    Sainmhíniú Studie, bei der sowohl der Prüfarzt als auch der Patient über die Zuordnung der Studienmedikation Bescheid wissen Tagairt Lexikon der Myelom Hilfe Österreich, s. v. "Offene Studie", http://www.myelom.at/de/lexikon/o.htm (6.7.2012)
    open-label study | open trial | open label trial | open-label trial | open-label studies | open label trials | open label studies | open trials | open-label trials | open label study
    en
    Sainmhíniú type of clinical study [ IATE:3543172 ] in which both the health providers and the patients are aware of the drug or treatment being given Tagairt COM-EN, based on:National Cancer Institute. Open label study http://www.cancer.gov/dictionary?cdrid=285990 [15.5.2012]
    Nóta See also:- clinical study [ IATE:3543172 ]- clinical trial [ IATE:1686971 ]
    essai ouvert
    fr
    Sainmhíniú type d'étude clinique au cours de laquelle aucun des participants (prescripteur et malade) n'est tenu dans l'ignorance du traitement administré Tagairt COM-FR, d'après:- Grand dictionnaire terminologique (2000) > Essai ouvert (11.1.2021)- Site de l'hôpital Nord France-Comté > La recherche > Recherche clinique > La recherche clinique à l'HNFC > Caractéristiques des essais cliniques (11.1.2021)
  19. INTERNATIONAL ORGANISATIONS|non-governmental organisations · SOCIAL QUESTIONS|health|medical science

    #566822

    IATE #1876500
    PRINTO Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Eagraíocht um Thástálacha Idirnáisiúnta sa Réamaiteolaíocht Phéidiatraiceach Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    PRINTO | Pediatric Rheumatology International Trials Organisation | Pediatric Rheumatology International Trials Organization
    en
    Nóta The Paediatric Rheumatology International Trials Organisation is a not for profit, non governmental, international research network. Founded in 1996. Initially included 14 European countries, with the goal to foster, facilitate and co-ordinate the development, conduct, analysis, and reporting of multi-centres, international clinical trials and/or outcome standardisation studies in children with paediatric rheumatic diseases (PRD).
  20. SOCIAL QUESTIONS|health|medical science|medical research · SOCIAL QUESTIONS|health|pharmaceutical industry|pharmaceutical product|medicament

    #597953

    IATE #3591762
    triail phragmatach Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Prüfung in der Praxis
    de
    pragmatic trial
    en
    Sainmhíniú clinical trial in which a treatment is prescribed and used as in normal daily practice Tagairt COM-Terminology Coordination, based on:Communication from the Commission - Pharmaceutical Strategy for Europe, COM(2020) 761 final
    essai clinique pragmatique | essai pragmatique
    fr
    Sainmhíniú essai thérapeutique ayant pour objectif d'évaluer l'intérêt pratique d'un nouveau traitement, déjà démontré comme efficace, en comparaison de ceux existant déjà, dans le but d'aider les praticiens à prendre des décisions thérapeutiques (ou la société, des décisions pour la santé publique) Tagairt COM-FR d'aprèsE Eschwège, G Bouvenot, Essais explicatifs ou pragmatiques, le dualisme (11.11.2021), La Revue de Médecine Interne, Volume 15, Issue 5, 1994, Pages 357-361, ISSN 0248-8663