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  1. #1671625

    Beidh an méid seo a leanas sa tuarascáil ar an measúnú riosca nó sa tuarascáil ar an measúnú comhcheangailte riosca:

    The risk assessment report or combined risk assessment report shall contain:

    Regulation (EU) 2017/2101 of the European Parliament and of the Council of 15 November 2017 amending Regulation (EC) No 1920/2006 as regards information exchange on, and an early warning system and risk assessment procedure for, new psychoactive substances

  2. #1747691

    Beidh an fhaisnéis seo a leanas sa tuarascáil measúnaithe riosca nó sa tuarascáil chomhcheangailte measúnaithe riosca:

    The risk assessment report or combined risk assessment report shall contain:

    Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulation (EC) No 1920/2006 as regards information exchange, early warning system and risk assessment procedure on new psychoactive substances

  3. #2853998

    Beidh an méid seo a leanas sa tuarascáil ar an measúnú riosca nó sa tuarascáil ar an measúnú comhcheangailte riosca:

    A risk assessment report or combined risk assessment report shall contain:

    Regulation (EU) 2023/1322 of the European Parliament and of the Council of 27 June 2023 on the European Union Drugs Agency (EUDA) and repealing Regulation (EC) No 1920/2006

  4. #2854010

    Cuirfidh an Ghníomhaireacht an tuarascáil ar an measúnú riosca nó an tuarascáil ar an measúnú comhcheangailte riosca faoi bhráid an Choimisiúin agus na mBallstát laistigh de 6 seachtaine ón iarraidh a fháil ón gCoimisiún tuarascáil ar an measúnú riosca a tharraingt suas de bhun mhír 1 nó tuarascáil ar an measúnú comhcheangailte riosca a tharraingt suas de bhun mhír 2.

    The Agency shall submit the risk assessment report or the combined risk assessment report to the Commission and the Member States within six weeks of receipt of the request from the Commission to draw up a risk assessment report pursuant to paragraph 1 or a combined risk assessment report pursuant to paragraph 2.

    Regulation (EU) 2023/1322 of the European Parliament and of the Council of 27 June 2023 on the European Union Drugs Agency (EUDA) and repealing Regulation (EC) No 1920/2006

  5. #306994

    Dréacht-tuarascáil maidir le measúnú

    Draft assessment report

    Regulation (EC) No 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC

  6. #437316

    (a) an tuarascáil mheasúnachta iomchuí arna hullmhú faoi alt 37, agus

    (a) the relevant assessment report prepared under section 37, and

    ADOPTION ACT 2010

  7. #437738

    (a) an tuarascáil mheasúnachta arna hullmhú faoi alt 37, agus

    (a) the assessment report prepared under section 37, and

    ADOPTION ACT 2010

  8. #437809

    (a) an tuarascáil mheasúnachta arna hullmhú faoi alt 37, agus

    (a) the assessment report prepared under section 37, and

    ADOPTION ACT 2010

  9. #516577

    (c) an tuarascáil measúnaithe deiridh ar an táirge bithicídeach.

    (c) the final assessment report on the biocidal product.

    Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

  10. #516911

    (e) an tuarascáil measúnaithe.

    (e) the assessment report.

    Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

  11. #516915

    (b) an tuarascáil measúnaithe.

    (b) the assessment report.

    Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

  12. #516969

    (c) an tuarascáil mheasúnaithe deiridh maidir leis an táirge bithicídeach.

    (c) the assessment report of the biocidal product.

    Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

  13. #592553

    Déanfar athbhreithniú ar an tuarascáil measúnúcháin gach trí bliana ar a laghad.

    The assessment report shall be reviewed at least every three years.

    Regulation (EU) No 167/2013 of the European Parliament and of the Council of 5 February 2013 on the approval and market surveillance of agricultural and forestry vehicles Text with EEA relevance

  14. #592554

    Má iarrtar amhlaidh, cuirfear an tuarascáil measúnúcháin in iúl don Choimisiún.

    The assessment report shall be communicated to the Commission upon request.

    Regulation (EU) No 167/2013 of the European Parliament and of the Council of 5 February 2013 on the approval and market surveillance of agricultural and forestry vehicles Text with EEA relevance

  15. #593703

    Déanfar athbhreithniú ar an tuarascáil measúnúcháin gach trí bliana ar a laghad.

    The assessment report shall be reviewed at least every three years.

    Regulation (EU) No 168/2013 of the European Parliament and of the Council of 15 January 2013 on the approval and market surveillance of two- or three-wheel vehicles and quadricycles Text with EEA relevance

  16. #593704

    Má iarrtar amhlaidh, cuirfear an tuarascáil measúnúcháin in iúl don Choimisiún.

    The assessment report shall be communicated to the Commission upon request.

    Regulation (EU) No 168/2013 of the European Parliament and of the Council of 15 January 2013 on the approval and market surveillance of two- or three-wheel vehicles and quadricycles Text with EEA relevance

  17. #611045

    An Ceathrú Tuarascáil Measúnaithe ón bPainéal Idir-rialtasach um Athrú Aeráide (IPCC), 2007 (www.ipcc.ch).

    IPCC 4th Assessment Report, 2007, (www.ipcc.ch).

    Regulation (EU) No 1291/2013 of the European Parliament and of the Council of 11 December 2013 establishing Horizon 2020 - the Framework Programme for Research and Innovation (2014-2020) and repealing Decision No 1982/2006/EC Text with EEA relevance

  18. #640873

    Tuarascáil measúnaithe — gnéithe a chumhdaítear i gCuid I

    Assessment report — Aspects covered by Part I

    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

  19. #640888

    Déanfaidh an Ballstát tuairiscithe tuarascáil measúnaithe a tharraingt suas.

    The reporting Member State shall draw up an assessment report.

    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

  20. #640890

    Beidh sa tuarascáil measúnaithe ceann amháin de na conclúidí seo a leanas i ndáil leis na gnéithe a dtugtar aghaidh orthu i gCuid I den tuarascáil measúnaithe:

    The assessment report shall contain one of the following conclusions concerning the aspects addressed in Part I of the assessment report:

    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

  21. #640915

    Tuarascáil measúnaithe — Gnéithe atá cumhdaithe i gCuid II

    Assessment report — Aspects covered by Part II

    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. #641023

    an mbaineann an modhnú substaintiúil le gné atá cumhdaithe ag Cuid I den tuarascáil measúnaithe;

    the substantial modification concerns an aspect covered by Part I of the assessment report;

    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

  23. #641032

    Modhnú substaintiúil ar ghné atá cumhdaithe ag Cuid I den tuarascáil measúnaithe a mheasúnú

    Assessment of a substantial modification of an aspect covered by Part I of the assessment report

    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

  24. #641052

    Cinneadh maidir leis an modhnú substaintiúil ar ghné atá cumhdaithe ag Cuid I den tuarascáil mheasúnaithe

    Decision on the substantial modification of an aspect covered by Part I of the assessment report

    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

  25. #641066

    cibé an mbaineann an modhnú substaintiúil le gné atá cumhdaithe ag Cuid II den tuarascáil mheasúnaithe;

    whether the substantial modification concerns an aspect covered by Part II of the assessment report;

    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

  26. #641084

    Modhnú substaintiúil ar ghnéithe atá cumhdaithe ag Cuid I agus ag Cuid II den tuarascáil mheasúnaithe

    Substantial modification of aspects covered by Parts I and II of the assessment report

    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

  27. #641088

    Measúnú ar mhodhnú substaintiúil ar ghnéithe atá cumhdaithe ag Cuid I agus ag Cuid II den tuarascáil mheasúnaithe — Measúnú ar na gnéithe atá cumhdaithe ag Cuid II den tuarascáil mheasúnaithe

    Assessment of a substantial modification of aspects covered by Parts I and II of the assessment reportAssessment of the aspects covered by Part II of the assessment report

    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

  28. #641585

    cumarsáid rúnda idir na Ballstáit a chosaint i ndáil le hullmhú na tuarascála measúnaithe;

    protecting confidential communication between Member States in relation to the preparation of the assessment report;

    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

  29. #675268

    Ba cheart go mbeadh an ríomh, nuair is féidir, bunaithe ar an gCeathrú Tuarascáil Mheasúnaithe arna glacadh ag an IPCC.

    The calculation should, where possible, be based on the Fourth Assessment Report adopted by the IPCC.

    Regulation (EU) No 517/2014 of the European Parliament and of the Council of 16 April 2014 on fluorinated greenhouse gases and repealing Regulation (EC) No 842/2006 Text with EEA relevance

  30. #675909

    Íosluach de réir an Ceathrú Tuarascáil Measúnaithe arna glacadh ag an bPainéal Idir-Rialtasach ar an Athrú Aeráide.

    Minimum value according to the Fourth Assessment Report adopted by the Intergovernmental Panel on Climate Change.

    Regulation (EU) No 517/2014 of the European Parliament and of the Council of 16 April 2014 on fluorinated greenhouse gases and repealing Regulation (EC) No 842/2006 Text with EEA relevance

  31. #728905

    Athbhreithneoidh an t-údarás ceadúcháin ainmniúcháin an tuarascáil mheasúnaithe gach trí bliana ar a laghad.

    The designating approval authority shall review the assessment report at least once every three years.

    Regulation (EU) 2016/1628 of the European Parliament and of the Council of 14 September 2016 on requirements relating to gaseous and particulate pollutant emission limits and type-approval for internal combustion engines for non-road mobile machinery, amending Regulations (EU) No 1024/2012 and (EU) No 167/2013, and amending and repealing Directive 97/68/EC (Text with EEA relevance)

  32. #728906

    Cuirfear an tuarascáil chuig an gCoimisiún ar iarraidh.

    The designating approval authority shall communicate the assessment report to the Commission upon the latter's request.

    Regulation (EU) 2016/1628 of the European Parliament and of the Council of 14 September 2016 on requirements relating to gaseous and particulate pollutant emission limits and type-approval for internal combustion engines for non-road mobile machinery, amending Regulations (EU) No 1024/2012 and (EU) No 167/2013, and amending and repealing Directive 97/68/EC (Text with EEA relevance)

  33. #734070

    Ba cheart do na húdaráis inniúla an tuarascáil mheasúnaithe a chur ar fáil go poiblí.

    Competent authorities should make the assessment report publicly available.

    Regulation (EU) 2016/2338 of the European Parliament and of the Council of 14 December 2016 amending Regulation (EC) No 1370/2007 concerning the opening of the market for domestic passenger transport services by rail (Text with EEA relevance )

  34. #734172

    Cuirfear an tuarascáil mheasúnaithe sin ar fáil go poiblí.

    The assessment report shall be made publicly available.

    Regulation (EU) 2016/2338 of the European Parliament and of the Council of 14 December 2016 amending Regulation (EC) No 1370/2007 concerning the opening of the market for domestic passenger transport services by rail (Text with EEA relevance )

  35. #742361

    Déanfaidh an t-údarás atá freagrach as comhlachtaí dá dtugtar fógra a thuarascáil measúnaithe dheiridh a tharraingt suas, ina mbeidh an méid seo a leanas:

    The authority responsible for notified bodies shall draw up its final assessment report which shall include:

    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

  36. #742566

    In éineacht leis an bhfógra sin beidh an tuarascáil ar an measúnú a dhéanfar ar an meastóireacht chliniciúil.

    That notification shall be accompanied by the clinical evaluation assessment report.

    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

  37. #746096

    Déanfaidh an t-údarás atá freagrach as comhlachtaí dá dtugtar fógra a thuarascáil mheasúnaithe dheiridh a tharraingt suas, ina mbeidh an méid seo a leanas:

    The authority responsible for notified bodies shall draw up its final assessment report which shall include:

    Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )

  38. #748007

    conclúidí a mheasúnuithe ar mheastóireachtaí feidhmíochta i dtuarascáil mheasúnaithe ar an meastóireacht feidhmíochta a dhoiciméadú go soiléir,

    clearly document the conclusions of its assessment of performance evaluation in a performance evaluation assessment report,

    Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )

  39. #1610688

    An Tuarascáil Measúnachta Buiséadaí. Meitheamh 2015.

    FISCAL ASSESSMENT REPORT. JUNE, 2015.

    Order of Business (Dáil Éireann/Seanad Éireann)

  40. #1610689

    An Tuarascáil Measúnachta Buiséadaí. Samhain 2015.

    FISCAL ASSESSMENT REPORT. NOVEMBER, 2015.

    Order of Business (Dáil Éireann/Seanad Éireann)

  41. #1671640

    Cuirfidh an Lárionad an tuarascáil ar an measúnú riosca nó an tuarascáil ar an measúnú comhcheangailte riosca faoi bhráid an Choimisiúin agus na mBallstát laistigh de 6 seachtaine ón iarraidh a fháil ón gCoimisiún tuarascáil ar an measúnú riosca a tharraingt suas.

    The Centre shall submit the risk assessment report or the combined risk assessment report to the Commission and the Member States within six weeks of receipt of the request from the Commission to draw up a risk assessment report.

    Regulation (EU) 2017/2101 of the European Parliament and of the Council of 15 November 2017 amending Regulation (EC) No 1920/2006 as regards information exchange on, and an early warning system and risk assessment procedure for, new psychoactive substances

  42. #1690690

    Anailís ar na torthaí agus tuarascáil measúnúcháin

    Analysis of findings and assessment report

    Regulation (EU) 2018/858 of the European Parliament and of the Council of 30 May 2018 on the approval and market surveillance of motor vehicles and their trailers, and of systems, components and separate technical units intended for such vehicles, amending Regulations (EC) No 715/2007 and (EC) No 595/2009 and repealing Directive 2007/46/EC (Text with EEA relevance.)

  43. #1690703

    Beidh an méid seo a leanas ar a laghad sa tuarascáil measúnúcháin:

    The assessment report shall include at least the following:

    Regulation (EU) 2018/858 of the European Parliament and of the Council of 30 May 2018 on the approval and market surveillance of motor vehicles and their trailers, and of systems, components and separate technical units intended for such vehicles, amending Regulations (EC) No 715/2007 and (EC) No 595/2009 and repealing Directive 2007/46/EC (Text with EEA relevance.)

  44. #1734073

    I gcás measúnú fabhrach, cuirfear san áireamh sa tuarascáil mheasúnaithe nó sa tuairim sin an méid seo a leanas:

    In case of a favourable assessment, that assessment report or opinion shall include the following:

    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)

  45. #1734250

    Déanfaidh an Ghníomhaireacht tuarascáil mheasúnaithe ina mbeidh an fhaisnéis dá dtagraítear in Airteagal 33.

    The competent authority shall prepare an assessment report containing the information referred to in Article 33.

    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)

  46. #1734251

    Cuirfidh an t-údarás inniúil an tuarascáil mheasúnaithe ar fáil go poiblí, tar éis dó aon fhaisnéis rúnda tráchtála a scriosadh.

    The competent authority shall make the assessment report publicly available, after deleting any commercially confidential information.

    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)

  47. #1734274

    Iarraidh ón iarratasóir ar athscrúdú ar an tuarascáil mheasúnaithe

    Request by the applicant for re-examination of the assessment report

    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)

  48. #1734278

    Déanfaidh an grúpa comhordúcháin athscrúdú ar an tuarascáil mheasúnaithe laistigh de 60 lá tar éis na forais mhionsonraithe don iarraidh ar athscrúdú ar an tuarascáil mheasúnaithe a fháil.

    Within 60 days of receipt of the detailed grounds for the request for re-examination of the assessment report, the coordination group shall re-examine the assessment report.

    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)

  49. #1734280

    Laistigh de 15 lá ón athscrúdú ar an tuarascáil mheasúnaithe, cuirfidh an Ballstát tagartha an tuarascáil mheasúnaithe ar aghaidh chuig an iarratasóir.

    Within 15 days of the re-examination of the assessment report, the competent authority in the reference Member State shall forward the assessment report to the applicant.

    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)

  50. #1734343

    an tuarascáil mheasúnaithe;

    the assessment report;

    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)