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  1. #1911838

    le haghaidh na substainte gníomhaí nó ábhar tosaigh, nó imoibrí nó idirmheánach den chuid na substainte gníomhaí;

    for the active substance or a starting material, reagent or intermediate of the active substance;

    Commission Implementing Regulation (EU) 2021/17 of 8 January 2021 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council (Text with EEA relevance)

  2. #2277458

    beidh substaint ghníomhach aon-náisiúnta ina substaint ghníomhach ilnáisiúnta.

    a mono-national active substance becomes a multi-national active substance.

    Commission Implementing Regulation (EU) 2022/20 of 7 January 2022 laying down rules for the application of Regulation (EU) No 536/2014 of the European Parliament and of the Council as regards setting up the rules and procedures for the cooperation of the Member States in safety assessment of clinical trials (Text with EEA relevance)

  3. #1735588

    Le haghaidh substaint ghníomhach, féadfaidh monaróir na substainte gníomhaí nó an t-iarratasóir a shocrú go gcuirfidh monaróir na substainte gníomhaí an fhaisnéis seo a leanas ar fáil i ndoiciméad ar leithligh go díreach do na húdaráis inniúla mar Mháistirchomhad maidir le Substaintí Gníomhacha:

    For a well-defined active substance, the active substance manufacturer or the applicant may arrange for the following information to be supplied in a separate document directly to the competent authorities by the manufacturer of the active substance as an Active Substance Master File:

    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)

  4. #2049609

    Le haghaidh substaint ghníomhach neamhbhitheolaíoch, féadfaidh an t-iarratasóir a shocrú go soláthróidh monaróir na substainte gníomhaí an fhaisnéis ar an tsubstaint ghníomhach i bpointe (2) go díreach do na húdaráis inniúla mar Mháistirchomhad maidir le Substaintí Gníomhacha.

    For a non-biological active substance, the applicant may arrange for the information on active substance in point (2) to be supplied directly to the competent authorities by the manufacturer of the active substance as an Active Substance Master File.

    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. #306726

    Ba cheart go gcuirfí na critéir seo i bhfeidhm maidir leis an gcéad fhormheas ar shubstaint ghníomhach faoin Rialachán seo.

    These criteria should be applied for the first approval of an active substance under this Regulation.

    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. #306735

    (13) Ar chúiseanna eitice, níor cheart go ndéanfaí measúnú ar shubstaint ghníomhach nó ar tháirge cosanta plandaí a bhunú ar thástálacha ná ar staidéir ina ndéantar an tsubstaint ghníomhach nó an táirge cosanta plandaí a thabhairt do dhaoine d’aon ghnó chun an "leibhéal iarmhairte gan bhreathnú" ar an duine a chinneadh i leith substainte gníomhaí.

    (13) For ethical reasons, the assessment of an active substance or a plant protection product should not be based on tests or studies involving the deliberate administration of the active substance or plant protection product to humans with the purpose of determining a human "no observed effect level" of an active substance.

    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

  7. #306928

    7. De mhaolú ar mhír 1, más rud é, ar bhonn fianaise doiciméadaí a chuirtear san áireamh san iarratas, gur gá substaint ghníomhach chun rialú a dhéanamh ar chontúirt thromchúiseach do shláinte plandaí nach féidir srian a chur uirthi ar aon slí infhaighte eile, lena n-áirítear modhanna neamhcheimiceacha, féadfar an tsubstaint ghníomhach sin a fhormheas go ceann tréimhse teoranta is gá chun rialú a dhéanamh ar an gcontúirt thromchúiseach sin ach ar tréimhse í nach faide ná cúig bliana fiú amháin más rud é nach gcomhlíonann sí na critéir a leagtar amach i bpointí 3.6.3, 3.6.4, 3.6.5 nó 3.8.2 d’Iarscríbhinn II, ar choinníoll go mbeidh úsáid na substainte faoi réir beart maolaithe riosca chun a áirithiú go ndéanfar íoslaghdú maidir le daoine agus maidir leis an gcomhshaol do theacht faoina lé.

    7. By way of derogation from paragraph 1, where on the basis of documented evidence included in the application an active substance is necessary to control a serious danger to plant health which cannot be contained by other available means including non-chemical methods, such active substance may be approved for a limited period necessary to control that serious danger but not exceeding five years even if it does not satisfy the criteria set out in points 3.6.3, 3.6.4, 3.6.5 or 3.8.2 of Annex II, provided that the use of the active substance is subject to risk mitigation measures to ensure that exposure of humans and the environment is minimised.

    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

  8. #306939

    (a) íosmhéid íonachta na substainte gníomhaí;

    (a) the minimum degree of purity of the active substance;

    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

  9. #306953

    1. Déanfaidh táirgeoir substainte gníomhaí iarratas ar fhormheas substainte gníomhaí nó iarratas ar leasú ar na coinníollacha a ghabhann le formheas substainte gníomhaí a chur faoi bhráid Ballstáit, (an Ballstát is rapóirtéir), mar aon le hachoimre agus sainchomhad iomlán, dá bhforáiltear in Airteagal 8(1) agus (2), nó cosaint atá réasúnaithe go heolaíoch ar an gcúis nár soláthraíodh codanna áirithe de na sainchomhaid sin, á léiriú go gcomhlíonann an tsubstaint ghníomhach na critéir formheasa dá bhforáiltear in Airteagal 4.

    1. An application for the approval of an active substance or for an amendment to the conditions of an approval shall be submitted by the producer of the active substance to a Member State, (the rapporteur Member State), together with a summary and a complete dossier as provided for in Article 8(1) and (2) or a scientifically reasoned justification for not providing certain parts of those dossiers, demonstrating that the active substance fulfils the approval criteria provided for in Article 4.

    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

  10. #307031

    (b) nach bhformheasfar substaint ghníomhach;

    (b) an active substance is not approved;

    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

  11. #307081

    (a) go ndéantar formheas substainte gníomhaí a athnuachan, faoi réir coinníollacha agus srianta nuair is iomchuí sin;

    (a) the approval of an active substance is renewed, subject to conditions and restrictions where appropriate;

    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

  12. #307083

    (b) nach ndéantar formheas substainte gníomhaí a athnuachan.

    (b) the approval of an active substance is not renewed.

    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

  13. #307110

    Chun críche mhír 2 go mír 6, is é atá i substaint ghníomhach ná substaint bhunata:

    For the purpose of paragraphs 2 to 6, a basic substance is an active substance which:

    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

  14. #307545

    (d) ainm agus méid gach substainte gníomhaí, gach teorantóra, nó gach sineirgígh atá ann;

    (d) the name and amount of each active substance, safener or synergist which it contains;

    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

  15. #307623

    (c) torthaí baisceanna táirgthe den tsubstaint ghníomhach, lena n-áirítear na heisíontais;

    (c) results of production batches of the active substance including impurities;

    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

  16. #307900

    Comhlíonann substaint ghníomhach, teorantóir nó sineirgíoch an critéar maidir le bithbhailiú más rud é:

    An active substance, safener or synergist fulfils the bioaccumulation criterion where there is:

    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

  17. #307904

    Comhlíonann substaint ghníomhach, teorantóir nó sineirgíoch an critéar maidir le hiompar fadraoin comhshaoil más rud é:

    An active substance, safener or synergist fulfils the potential for long-range environmental transport criterion where:

    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

  18. #307912

    Comhlíonann substaint ghníomhach, teorantóir nó sineirgíoch an critéar maidir le marthanacht más rud é:

    An active substance, safener or synergist fulfils the persistence criterion where:

    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

  19. #307924

    Comhlíonann substaint ghníomhach, teorantóir nó sineirgíoch an critéar maidir le tocsaineacht más rud é:

    An active substance, safener or synergist fulfils the toxicity criterion where:

    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

  20. #307931

    Comhlíonann substaint ghníomhach, teorantóir nó sineirgíoch an critéar maidir le "an-mharthanach" más rud é:

    An active substance, safener or synergist fulfils the "very persistent" criterion where:

    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

  21. #328506

    go liostaítear an tsubstaint ghníomhach in Iarscríbhinn IV.

    the active substance is listed in Annex IV.

    Regulation (EC) No 299/2008 of the European Parliament and of the Council of 11 March 2008 amending Regulation (EC) No 396/2005 on maximum residue levels of pesticides in or on food and feed of plant and animal origin, as regards the implementing powers conferred on the Commission

  22. #346633

    Ní fhéadfar substaint atá gníomhach ó thaobh na cógaseolaíochta de a úsáid i mbia-ainmhithe ach má mheasúnaítear go fabhrach í.

    A pharmacologically active substance may be used in food-producing animals only if evaluated favourably.

    Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council

  23. #346874

    Bia de thionscnamh ainmhíoch ina bhfuil substaint atá gníomhach ó thaobh na cógaseolaíochta de:

    Food of animal origin containing residues of a pharmacologically active substance:

    Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council

  24. #516025

    (a) íosmhéid íonachta na substainte gníomhaí;

    (a) the minimum degree of purity of the active substance;

    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

  25. #516031

    (g) coinníollacha eile ar leith bunaithe ar mheastóireacht a dhéanamh ar an bhfaisnéis a bhaineann leis an substaint ghníomhach sin;

    (g) other particular conditions based on the evaluation of the information related to that active substance;

    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

  26. #516032

    (h) dáta formheasa agus dáta éaga fhormheas na substainte gníomhaí.

    (h) the date of approval and the expiry date of the approval of the active substance.

    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

  27. #516056

    (a) sainchomhad don tsubstaint ghníomhach lena gcomhlíontar na ceanglais a leagtar amach in Iarscríbhinn II;

    (a) a dossier for the active substance satisfying the requirements set out in Annex II;

    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

  28. #516099

    Substaint ghníomhach a fhormheas

    Approval of an active substance

    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

  29. #516125

    FORMHEAS SUBSTAINTE GNÍOMHAÍ A ATHNUACHAN AGUS A ATHBREITHNIÚ

    RENEWAL AND REVIEW OF APPROVAL OF AN ACTIVE SUBSTANCE

    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

  30. #516157

    (b) cinneadh cur chun feidhme á rá nach ndéantar formheas substainte gníomhaí a athnuachan.

    (b) an implementing decision that the approval of an active substance is not renewed.

    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

  31. #516165

    Athbhreithniú ar fhormheas substainte gníomhaí

    Review of approval of an active substance

    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

  32. #516619

    (b) aon sonraí a léiríonn poitéinseal na substainte gníomhaí frithsheasmhacht a fhorbairt;

    (b) any data indicating the potential of the active substance for the development of resistance;

    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

  33. #516831

    1. I gcás ina bhfuil an tréimhse chosanta faisnéise ábhartha i gcomhréir le hAirteagal 60 éagtha i gcás substainte gníomhaí, féadfaidh an t-údarás inniúil glactha nó an Ghníomhaireacht aontú go bhféadfaidh iarratasóir a bheadh ann ina dhiaidh sin tagairt a dhéanamh do shonraí a sholáthair an chéad iarratasóir sa mhéid is gur féidir leis an iarratasóir a bheadh ann ina dhiaidh sin fianaise a sholáthar gur coibhéiseach go teicniúil an tsubstaint ghníomhach leis an substaint ghníomhach dá bhfuil an tréimhse chosanta faisnéise éagtha, lena n-airítear an leibhéal íonachta agus saghas aon eisíontas ábhartha.

    1. Where the relevant data protection period according to Article 60 has expired in relation to an active substance, the receiving competent authority or the Agency may agree that a subsequent applicant for authorisation may refer to data provided by the first applicant in so far as the subsequent applicant can provide evidence that the active substance is technically equivalent to the active substance for which the data protection period has expired, including the degree of purity and the nature of any relevant impurities.

    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

  34. #516836

    (b) na sonraí is gá chun an tsubstaint ghníomhach a shainaithint agus chun coibhéis theicniúil na substainte gníomhaí a chruthú;

    (b) the data needed to identify the active substance and to establish technical equivalence of the active substance;

    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

  35. #516878

    (c) ainm agus seoladh mhonaróir na substainte gníomhaí;

    (c) the name and address of the active substance manufacturer;

    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

  36. #516881

    (f) aon mhodhanna chun an tsubstaint ghníomhach nó an táirge bithicídeach a fhágáil neamhdhíobhálach;

    (f) any methods for rendering the active substance or biocidal product harmless;

    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

  37. #516931

    (a) céannacht gach substainte gníomhaí agus a thiúchan de réir aonad méadrach;

    (a) the identity of every active substance and its concentration in metric units;

    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

  38. #517142

    Sonrófar an dáta formheasa sna rialacháin lena bhformheastar substaint ghníomhach.

    Regulations approving an active substance shall specify the date of approval.

    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

  39. #517187

    Bearta idirthréimhseacha a bhaineann le rochtain ar shainchomhad na substainte gníomhaí

    Transitional measures concerning access to the active substance dossier

    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

  40. #517264

    Liostaítear sa tábla thíos an fhaisnéis a cheanglaítear chun tacú le substaint ghníomhach a fhormheas.

    Information required to support the approval of an active substance is listed in the table below.

    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

  41. #517267

    2.CÉANNACHT NA SUBSTAINTE GNÍOMHAÍ

    2.IDENTITY OF THE ACTIVE SUBSTANCE

    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

  42. #517268

    3.AIRÍONNA FISICEACHA AGUS CEIMICEACHA NA SUBSTAINTE GNÍOMHAÍ

    3.PHYSICAL AND CHEMICAL PROPERTIES OF THE ACTIVE SUBSTANCE

    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

  43. #517311

    Liostaítear sa tábla thíos an fhaisnéis atá ag teastáil chun tacú le substaint ghníomhach a fhormheas.

    Information required to support the approval of an active substance is listed in the table below.

    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

  44. #517330

    [4] An fhaisnéis a chuirtear ar fáil, ba cheart gurb i gcás na substainte gníomhaí íonaithe atá sa tsonraíocht luaite a sholáthraítear í nó i gcás na substainte gníomhaí mar a monaraíodh í, má tá sin difriúil.

    [4] The information provided should be for the purified active substance of stated specification or for the active substance as manufactured, if different.

    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

  45. #517331

    [5] Ba cheart gurb í an fhaisnéis a sholáthraítear an fhaisnéis don tsubstaint ghníomhach íonaithe atá sa tsonraíocht luaite.

    [5] The information provided should be for the purified active substance of stated specification.

    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

  46. #517722

    - aon airíonna speisialta eile de chuid na substainte gníomhaí nó de chuid na substainte ar údar imní í,

    - any other special properties of the active substance or substance of concern,

    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

  47. #624257

    A bhfuil nicil nó comhdhúile nicile iontu mar shubstaint ghníomhach

    With nickel or nickel compounds as the active substance

    REGULATION (EU) No 374/2014 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 16 April 2014 on the reduction or elimination of customs duties on goods originating in Ukraine

  48. #624258

    A bhfuil miotail lómhar nó comhdhúile de mhiotail lómhara iontu mar shubstaint ghníomhach

    With precious metal or precious-metal compounds as the active substance

    REGULATION (EU) No 374/2014 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 16 April 2014 on the reduction or elimination of customs duties on goods originating in Ukraine

  49. #633703

    I gcás táirgí bithicídeacha a bhfuil níos mó ná substaint ghníomhach amháin iontu, déanfar na hiarratais a chur isteach tráth nach déanaí ná dáta formheasa na substainte gníomhaí deireanaí don chineál sin táirge.

    In the case of biocidal products containing more than one active substance, applications shall be submitted no later than the date of approval of the last active substance for that product-type.

    Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market Text with EEA relevance

  50. #633728

    Bearta idirthréimhseacha a bhaineann le rochtain ar shainchomhad na substainte gníomhaí

    Transitional measures concerning access to the active substance dossier

    Regulation (EU) No 334/2014 of the European Parliament and of the Council of 11 March 2014 amending Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products, with regard to certain conditions for access to the market Text with EEA relevance