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trialach

1,795 results in 377 documents

  1. #1735983

    Ach amháin má tá údar maith leis, déanfar trialacha cliniciúla le hainmhithe cóimheasa (trialacha cliniciúla rialaithe).

    Unless justified, clinical trials shall be carried out with control animals (controlled clinical trials).

    Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)

  2. #1736304

    Nuair nach féidir trialacha saotharlainne tacaíocht a thabhairt d’éifeachtúlacht, d’fhéadfadh trialacha allamuigh a bheith inghlactha.

    Where laboratory trials cannot be supportive of efficacy, the performance of field trials alone may be acceptable.

    Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)

  3. #2049892

    Ach amháin mura bhfuil údar leis, déanfar trialacha cliniciúla le hainmhithe cóimheasa (trialacha cliniciúla rialaithe).

    Unless otherwise justified, clinical trials shall be carried out with control animals (controlled clinical trials).

    Commission Delegated Regulation (EU) 2021/805 of 8 March 2021 amending Annex II to Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  4. #2050243

    Déanfar trialacha cliniciúla (trialacha allamuigh) i gcomhréir le prionsabail sheanbhunaithe an dea-chleachtais chliniciúil (DCC).

    Clinical trials (field trials) shall be conducted in compliance with established principles of good clinical practice (GCP).

    Commission Delegated Regulation (EU) 2021/805 of 8 March 2021 amending Annex II to Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  5. #2409395

    Is trialacha allamuigh in úlloird a bhí sna trialacha a rinne an t-iarratasóir.

    The tests performed by the applicant were field trials conducted in orchards.

    Commission Implementing Decision (EU) 2022/1494 of 7 September 2022 on the unresolved objections regarding the conditions for granting an authorisation for the biocidal product Mouskito Spray in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022) 6264) (Text with EEA relevance)

  6. #2410080

    Is trialacha allamuigh in úlloird a bhí sna trialacha a rinne an t-iarratasóir.

    The tests performed by the applicant were field trials conducted in orchards.

    Commission Implementing Decision (EU) 2022/1515 of 8 September 2022 on the unresolved objections regarding the conditions for granting an authorisation for the biocidal product Mouskito Junior Lotion in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022)6279) (Text with EEA relevance)

  7. #2617367

    Moltar gur cheart trialacha luasmhoillithe saor-rothlaithe a dhéanamh go comhleantach gan moill mhíchuí idir trialacha.

    It is recommended that coastdown runs should be conducted successively without undue delay between runs.

    UN Regulation No 154 – Uniform provisions concerning the approval of light duty passenger and commercial vehicles with regards to criteria emissions, emissions of carbon dioxide and fuel consumption and/or the measurement of electric energy consumption and electric range (WLTP) [2022/2124]

  8. #148033

    Tabharfar fógra trialach sula gcuirfear an chaingean síos i gcomhair trialach.

    Notice of trial shall be given before setting down the action for trial.

    Statutory Instruments: 1980

  9. #254376

    Fógra Trialach/Fógra chun dáta a shocrú le haghaidh Trialach

    Notice of Trial/Notice to fix a date for Trial

    S.I. No. 510 of 2001: The Circuit Court Rules

  10. #640830

    Ciallaíonn “fionraíocht na trialach cliniciúla” Ballstát do bhriseadh isteach ar stiúradh na trialach cliniciúla;

    ‘Suspension of a clinical trial’ means interruption of the conduct of a clinical trial by a Member State;

    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 Text with EEA relevance

  11. #641258

    Deireadh trialach cliniciúla, stad sealadach agus foirceannadh trialach cliniciúla go luath agus taisceadh na dtorthaí

    End of a clinical trial, temporary halt and early termination of a clinical trial and submission of the results

    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 Text with EEA relevance

  12. #642061

    Sainaithint trialach cliniciúla (lena n-áirítear teideal na trialach agus uimhir prótacail);

    Clinical trial identification (including title of the trial and protocol number);

    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 Text with EEA relevance

  13. #1453479

    (a) cuspóirí na trialach beartaithe agus pleanáil agus eagrú na trialach sin;

    ( a ) the objectives of the proposed trial and its planning and organisational structure;

    Number 28 of 1987: CONTROL OF CLINICAL TRIALS ACT, 1987

  14. #1560531

    Socróidh an Dlísheomra Trialach dáta le haghaidh na trialach ansin.

    The Trial Chamber shall then set the date for trial.

    Number 40 of 1998: INTERNATIONAL WAR CRIMES TRIBUNALS ACT, 1998

  15. #1560942

    Socróidh an Dlísheomra Trialach dáta le haghaidh na trialach ansin.

    The Trial Chamber shall then set the date for trial.

    Number 40 of 1998: INTERNATIONAL WAR CRIMES TRIBUNALS ACT, 1998

  16. #1700704

    Déanfar fógra trialach a thabhairt sula gcuirfear an chaingean síos i gcomhair trialach.

    Notice of trial shall be given before setting down the action for trial.

    S.I. No. 15 of 1986: The Rules of the Superior Courts

  17. #641780

    tuairisc ar chineál na trialach cliniciúla atá le stiúradh agus plé ar dhearadh na trialach cliniciúla (lena n-áirítear scéimléaráid de dhearadh, nósanna imeachta agus céimeanna na trialach, más ábhartha);

    a description of the type of clinical trial to be conducted and a discussion of the trial design (including a schematic diagram of trial design, procedures and stages, if relevant);

    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 Text with EEA relevance

  18. #1736272

    Beidh leas na n-ainmhithe trialach faoi réir maoirsiú tréidliachta agus cuirfear go hiomlán san áireamh é i rith mionsaothrú aon phrótacail trialach agus le linn na trialach.

    The welfare of the trial animals shall be subject to veterinary supervision and shall be taken fully into consideration during the elaboration of any trial protocol and throughout the conduct of the trial.

    Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)

  19. #2049536

    Beidh leas na n-ainmhithe trialach faoi réir maoirsiú tréidliachta agus cuirfear go hiomlán san áireamh é i rith mionsaothrú aon phrótacail trialach agus le linn na trialach.

    The welfare of the trial animals shall be subject to veterinary supervision and shall be taken fully into consideration during the elaboration of any trial protocol and throughout the conduct of the trial.

    Commission Delegated Regulation (EU) 2021/805 of 8 March 2021 amending Annex II to Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  20. #230576

    Ó cuireadh an cúisí á chimiú/á cimiú chun a thrialach/a trialach:

    The accused being committed for trial:

    S.I. No. 93 of 1997: The District Court Rules

  21. #641762

    uimhir thrialach AE;

    the EU trial number;

    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 Text with EEA relevance

  22. #1159494

    (a) ina gcuirfear duine chun a thrialach i gcion indíotáilte, agus

    ( a ) a person is returned for trial for an indictable offence, and

    Number 12 of 1962: CRIMINAL JUSTICE (LEGAL AID) ACT, 1962

  23. #1159506

    (c) (i) gur ar chúiseamh i ndúnmharú a chuirfear chun a thrialach é, nó

    [GA] (i) the return for trial is upon a charge of murder, or

    Number 12 of 1962: CRIMINAL JUSTICE (LEGAL AID) ACT, 1962

  24. #1494420

    (ii) go gcuirfear chun a thrialach é mar gheall ar aon chion den sórt sin, nó

    (ii) committed for trial for any such offence, or

    Number 18 of 1989: CHILDREN ACT, 1989

  25. #1700698

    Mura dtabharfaidh an gearánaí in aon chaingean fógra trialach laistigh de shé sheachtain tar éis dheireadh na bpléadálacha, nó laistigh de cibé tréimhse fhadaithe ama a lamhálfaidh an Chúirt, féadfaidh an cosantóir, roimh fhógra trialach arna thabhairt ag an ngearánaí, fógra trialach a thabhairt (ar fógra é le haghaidh trialach le giúiré, i gcásanna ina mbeidh an gearánaí i dteideal giúiré, de cheart), nó féadfaidh sé a iarraidh ar an gCúirt an chaingean a dhíbhe d'uireasa í a thabhairt ar aghaidh; agus ar an iarratas sin a éisteacht féadfaidh an Chúirt a ordú an chaingean a dhíbhe dá réir sin, nó féadfaidh sí cibé ordú eile a dhéanamh is cóir leis an gCúirt ar cibé téarmaí is cóir léi.

    If the plaintiff in any action does not within six weeks after the close of the pleadings, or within such extended time as the Court may allow, give notice of trial, the defendant may, before notice of trial given by the plaintiff, give notice of trial (which, in cases where the plaintiff is entitled as of right to a jury, shall be for trial with a jury), or may apply to the Court to dismiss the action for want of prosecution; and on the hearing of such application, the Court may order the action to be dismissed accordingly, or may make such other order, and on such terms, as to the Court may seem just.

    S.I. No. 15 of 1986: The Rules of the Superior Courts

  26. #1993624

    Taighde agus forbairt thrialach ar eolaíochtaí nádúrtha agus innealtóireacht (Cód NACE 72.1)

    Research and experimental development on natural sciences and engineering (NACE Code 72.1)

    Commission Decision (EU) 2021/2054 of 8 November 2021 on the sectoral reference document on best environmental management practices, environmental performance indicators and benchmarks of excellence for the telecommunications and information and communication technologies (ICT) services sector for the purposes of Regulation (EC) No 1221/2009 of the European Parliament and of the Council (Text with EEA relevance)

  27. #2708460

    Taighde agus forbairt thrialach ar eolaíochtaí aiceanta agus innealtóireacht

    Research and experimental development on natural sciences and engineering

    Commission Delegated Regulation (EU) 2023/137 of 10 October 2022 amending Regulation (EC) No 1893/2006 of the European Parliament and of the Council establishing the statistical classification of economic activities NACE Revision 2 (Text with EEA relevance)

  28. #2708461

    Taighde agus forbairt thrialach ar eolaíochtaí sóisialta agus ar na daonnachtaí

    Research and experimental development on social sciences and humanities

    Commission Delegated Regulation (EU) 2023/137 of 10 October 2022 amending Regulation (EC) No 1893/2006 of the European Parliament and of the Council establishing the statistical classification of economic activities NACE Revision 2 (Text with EEA relevance)

  29. #295400

    Staidéir thrialacha agus anailísí costais agus tairbhe

    Pilot studies and cost-benefit analyses

    Regulation (EC) No 1338/2008 of the European Parliament and of the Council of 16 December 2008 on Community statistics on public health and health and safety at work

  30. #510637

    tionscadail, lena n-áirítear tionscadail thrialacha;

    projects, including test projects;

    Regulation (EU) No 1255/2011 of the European Parliament and of the Council of 30 November 2011 establishing a Programme to support the further development of an Integrated Maritime Policy (Text with EEA relevance)

  31. #510643

    gníomhaíochtaí a bhaineann le huirlisí crosghearrthacha, lena n-áirítear tionscadail thrialacha.

    actions relating to cross-cutting tools, including test projects.

    Regulation (EU) No 1255/2011 of the European Parliament and of the Council of 30 November 2011 establishing a Programme to support the further development of an Integrated Maritime Policy (Text with EEA relevance)

  32. #641114

    urraitheoir, imscrúdaitheoirí, daoine is ábhar ionchasacha, daoine is ábhar, agus suíomhanna um thrialacha cliniciúla;

    the sponsor, investigators, potential subjects, subjects, and clinical trial sites;

    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 Text with EEA relevance

  33. #641629

    Féadfaidh na Ballstáit táillí laghdaithe a bhunú do thrialacha cliniciúla neamhthráchtála.

    Member States may establish reduced fees for non-commercial clinical trials.

    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 Text with EEA relevance

  34. #641872

    Sonraí ó thrialacha cliniciúla a rinneadh roimhe seo agus sonraí ó thaithí an duine

    Data from previous clinical trials and human experience

    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 Text with EEA relevance

  35. #671292

    tionscadail, lena n-áirítear tionscadail thrialacha agus tionscadail comhair;

    projects, including test projects and cooperation projects;

    Regulation (EU) No 508/2014 of the European Parliament and of the Council of 15 May 2014 on the European Maritime and Fisheries Fund and repealing Council Regulations (EC) No 2328/2003, (EC) No 861/2006, (EC) No 1198/2006 and (EC) No 791/2007 and Regulation (EU) No 1255/2011 of the European Parliament and of the Council

  36. #1592965

    Tairiscint maidir leis an gConradh um Chosc Cuimsitheach ar Thrialacha Núicléacha

    1) MOTION RE COMPREHENSIVE NUCLEAR TEST BAN TREATY.

    Order of Business (Dáil Éireann/Seanad Éireann)

  37. #1593611

    cosc cuimsitheach ar thrialacha núicleácha

    a comprehensive nuclear test ban

    Order of Business (Dáil Éireann/Seanad Éireann)

  38. #1593612

    cosc cuimsitheach ar thrialacha núicléacha

    a comprehensive nuclear test ban

    Order of Business (Dáil Éireann/Seanad Éireann)

  39. #1600829

    Tuarascáil ar Thrialacha maidir le Vacsaín Chliniciúil.

    CLINICAL VACCINE TRIALS REPORT.

    Order of Business (Dáil Éireann/Seanad Éireann)

  40. #1601907

    Conradh um Chosc Cuimsitheach ar Thrialacha Núicléacha.

    COMPREHENSIVE NUCLEAR TEST BAN TREATY.

    Order of Business (Dáil Éireann/Seanad Éireann)

  41. #1621485

    Tairiscint maidir leis an Tuarascáil ar Thrialacha maidir le Vacsaín Chliniciúil a chur chun Comhchoiste.

    MOTION RE REFERRAL TO JOINT COMMITTEE OF THE REPORT ON CLINICAL VACCINE TRIALS.

    Order of Business (Dáil Éireann/Seanad Éireann)

  42. #1630578

    Rún ag bunú an Choimisiúin Ullmhúcháin d'Eagraíocht an Chonartha um Chosc Cuimsitheach ar Thrialacha Núicléacha.

    RESOLUTION ESTABLISHING THE PREPARATORY COMMISSION FOR THE COMPREHENSIVE NUCLEAR TEST-BAN TREATY ORGANIZATION.

    Order of Business (Dáil Éireann/Seanad Éireann)

  43. #1634680

    Ráitis ar Thuarascáil ar Thrialacha maidir le Vacsaín Chliniciúil. Rinneadh Ráitis ar Thuarascáil ar Thrialacha maidir le Vacsaín Chliniciúil.

    STATEMENTS ON CLINICAL VACCINE TRIALS REPORT. STATEMENTS WERE MADE ON CLINICAL VACCINE TRIALS REPORT.

    Order of Business (Dáil Éireann/Seanad Éireann)

  44. #2063448

    Scagadh/meastóireacht ar riachtanais foghlama aonair bunaithe ar thrialacha gairmiúla agus/nó agallaimh ghairmiúla

    Screening/evaluation of individual learning needs based on professional tests and/or interviews

    Commission Delegated Regulation (EU) 2021/859 of 4 February 2021 supplementing Regulation (EU) 2019/1700 of the European Parliament and of the Council by specifying the number and titles of the variables for the data set in the education and training domain (Text with EEA relevance)

  45. #2063963

    Scagadh/meastóireacht ar riachtanais foghlama aonair bunaithe ar thrialacha gairmiúla agus/nó agallaimh ghairmiúla

    Screening/evaluation of individual learning needs based on professional tests and/or interviews

    Commission Implementing Regulation (EU) 2021/861 of 21 May 2021 specifying the technical items of the data set and establishing the technical formats for transmission of information on the organisation of a sample survey in the education and training domain pursuant to Regulation (EU) 2019/1700 of the European Parliament and of the Council (Text with EEA relevance)

  46. #2292123

    saineolaithe eile ar thrialacha cliniciúla a dhéanfaidh ionadaíocht thar ceann údaráis náisiúnta inniúla do tháirgí náisiúnta.

    other clinical trial experts who represent national competent authorities for medicinal products.

    Regulation (EU) 2022/123 of the European Parliament and of the Council of 25 January 2022 on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and medical devices (Text with EEA relevance)

  47. #2365026

    Sábháilteacht fhorlíonadh ríse giosta dheirg: Athbhreithniú córasach agus meitea-anailísiú ar thrialacha rialaithe randamaithe.

    Safety of red yeast rice supplementation: A systematic review and meta-analysis of randomized controlled trials.

    Commission Regulation (EU) 2022/860 of 1 June 2022 amending Annex III to Regulation (EC) No 1925/2006 of the European Parliament and of the Council as regards monacolins from red yeast rice (Text with EEA relevance)

  48. #2909088

    TACAÍOCHT DO GHNÍOMHAÍOCHTAÍ CHOIMISIÚN ULLMHÚCHÁIN EAGRAÍOCHT AN CHONARTHA UM CHOSC CUIMSITHEACH AR THRIALACHA NÚICLÉACHA (CTBTO)

    SUPPORT FOR THE ACTIVITIES OF THE PREPARATORY COMMISSION OF THE COMPREHENSIVE NUCLEAR-TEST-BAN TREATY ORGANIZATION (CTBTO)

    Council Decision (CFSP) 2023/2064 of 25 September 2023 on Union support for the activities of the Preparatory Commission of the Comprehensive Nuclear-Test-Ban Treaty Organization (CTBTO) in order to strengthen its monitoring and verification capabilities

  49. #3131849

    Bailíochtú tosaigh trí thrialacha comhoibríocha

    Initial validation through collaborative trials

    Commission Implementing Regulation (EU) 2023/2782 of 14 December 2023 laying down the methods of sampling and analysis for the control of the levels of mycotoxins in food and repealing Regulation (EC) No 401/2006

  50. #3131879

    Modhanna, ar bailíochtaíodh iad cheana féin trí thrialacha comhoibríocha, a fhíorú

    Verification of methods already validated through collaborative trials

    Commission Implementing Regulation (EU) 2023/2782 of 14 December 2023 laying down the methods of sampling and analysis for the control of the levels of mycotoxins in food and repealing Regulation (EC) No 401/2006