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  1. #743833

    prionsabail oibriúcháin na feiste agus léiriú eolaíoch ar a modh gníomhaíochta, más gá;

    principles of operation of the device and its mode of action, scientifically demonstrated if necessary;

    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. )

  2. #1945222

    fágfar as an áireamh tuilleadh tástála ar ainmhithe veirteabracha chun na críche sin i gcás an mhodha gníomhaíochta sin;

    further testing on vertebrate animals for that effect shall be omitted for that mode of action,

    Commission Delegated Regulation (EU) 2021/525 of 19 October 2020 amending Annexes II and III to Regulation (EU) No 528/2012 of the European Parliament and of the Council concerning the making available on the market and use of biocidal products (Text with EEA relevance)

  3. #1945223

    féadfar tuilleadh tástála nach mbaineann le hainmhithe veirteabracha a fhágáil as an áireamh i gcás an mhodha gníomhaíochta sin.

    further testing not involving vertebrate animals may be omitted for that mode of action.

    Commission Delegated Regulation (EU) 2021/525 of 19 October 2020 amending Annexes II and III to Regulation (EU) No 528/2012 of the European Parliament and of the Council concerning the making available on the market and use of biocidal products (Text with EEA relevance)

  4. #2512491

    Modh gníomhaíochta ar an spriocorgánach agus an raon óstaigh

    Mode of action on the target organism and host range

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)

  5. #2513147

    Modh gníomhaíochta ar an spriocorgánach

    Mode of action on the target organism

    Commission Regulation (EU) 2022/1440 of 31 August 2022 amending Regulation (EU) No 284/2013 as regards the information to be submitted for plant protection products and the specific data requirements for plant protection products containing micro-organisms (Text with EEA relevance)

  6. #2514208

    modh gníomhaíochta;

    mode of action;

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  7. #2514216

    an modh gníomhaíochta atá aige;

    its mode of action;

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  8. #3042464

    Mar gheall ar mhodh gníomhaíochta ciorómaisín, tosaíonn rialú larbhach éifeachtach go mall.

    Due to the mode of action of cyromazine, effective larval control starts delayed.

    Commission Implementing Regulation (EU) 2023/2649 of 28 November 2023 granting a Union authorisation for the single biocidal product Hokoex in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

  9. #2512495

    I gcás modh gníomhaíochta bunaithe ar mheitibilít arb údar imní í de tháirgeadh an mhiocrorgánaigh atá faoi mheasúnú agus a shainaithnítear mar rud a cheanglaítear faoi phointe 2.8, cuirfear ar fáil faisnéis ó litríocht eolaíoch a ndearnadh athbhreithniú piaraí uirthi nó aon fhoinse iontaofa eile maidir le modh is dócha gníomhaíochta na meitibilíte arb údar imní í agus bealach is dóchúil nochta an spriocorgánaigh chuig an mheitibilít arb údar imní í.

    In case of a mode of action based on a metabolite of concern produced by the micro-organism under assessment and identified as required by point 2.8, information from scientific peer-reviewed literature or any other reliable source on likely mode of action of the metabolite of concern and likely exposure route of the target organism to the metabolite of concern shall be provided.

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)

  10. #284824

    Nuair a bhíonn táirgí bunaithe ar chealla inmharthana nó ar fhíocháin inmharthana, ba cheart a mheas gurb é an gníomh cógaseolaíoch, imdhíoneolaíoch nó meitibileach an príomh-mhodh gníomhaíochta.

    When products are based on viable cells or tissues, the pharmacological, immunological or metabolic action should be considered as the principal mode of action.

    Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004

  11. #292586

    Déanfar faisnéis maidir le substaintí nó meascáin a bhaineann leis an tsubstaint nó meascán atá á aicmiú nó á haicmiú a mheas mar fhaisnéis atá iomchuí, chomh maith le torthaí staidéir maidir le suíomh gníomhaíochta agus meicníocht nó modh gníomhaithe.

    Information on substances or mixtures related to the substance or mixture being classified shall be considered as appropriate, as well as site of action and mechanism or mode of action study results.

    Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006

  12. #292595

    I gcás ina mbeidh fianaise eolaíoch ann nach mbaineann an mheicníocht ghníomhaithe nó an modh gníomhaithe le daoine, níor chóir an tsubstaint nó meascán a aicmiú.

    When there is scientific evidence that the mechanism or mode of action is not relevant to humans, the substance or mixture should not be classified.

    Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006

  13. #293925

    (k) modh gníomhaíochta agus an bhaint atá aige le daoine, amhail cíteatocsaineacht a spreagann fás, mitigineas, cosc imdhíonachta, só-ghineacht.

    (k) mode of action and its relevance for humans, such as cytotoxicity with growth stimulation, mitogenesis, immunosuppression, mutagenicity.

    Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006

  14. #741703

    Agus cinneadh á dhéanamh cibé an faoi Threoir 2001/83/EC nó faoin Rialachán seo a thagann an táirge, tabharfar aird ar leith ar phríomh-mhodh gníomhaíochta an táirge;

    In deciding whether a product falls under Directive 2001/83/EC or under this Regulation, particular account shall be taken of the principal mode of action of the product;

    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. )

  15. #1735774

    tástálacha breise a d’fhéadfadh gá a bheith leo ag brath ar chúiseanna imní sonracha amhail iadsan a bhaineann le struchtúr, aicme agus modh gníomhaíochta substainte gníomhaí/substaintí gníomhacha;

    additional tests that may be required depending on specific toxicological concerns such as those associated with the structure, class, and mode of action of the active substance(s);

    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)

  16. #1945221

    I gcás ina mbeidh fianaise leordhóthanach ar fáil chun a chinneadh gurb ann nó nach ann do mhodh gníomhaíochta réabtha inchrínigh ar leith:

    Where sufficient weight of evidence to conclude on the presence or absence of a particular endocrine disrupting mode of action is available:

    Commission Delegated Regulation (EU) 2021/525 of 19 October 2020 amending Annexes II and III to Regulation (EU) No 528/2012 of the European Parliament and of the Council concerning the making available on the market and use of biocidal products (Text with EEA relevance)

  17. #2049853

    Tabharfar tuairisc leormhaith ar an modh gníomhaíochta agus ar na héifeachtaí cógaseolaíocha ar a bhfuil an t-iarratas molta bunaithe, i gcleachtas, lena n-áirítear éifeachtaí tánaisteacha (más ann dóibh).

    The mode of action and the pharmacological effects on which the recommended application is based in practice shall be adequately described, including secondary effects (if any).

    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)

  18. #2050124

    Tabharfar tuairisc leormhaith ar an modh gníomhaíochta agus ar na héifeachtaí cógaseolaíocha ar a bhfuil an t-iarratas molta bunaithe, i gcleachtas, lena n-áirítear éifeachtaí tánaisteacha (más ann dóibh).

    The mode of action and the pharmacological effects on which the recommended application in practice is based shall be adequately described, including secondary effects (if any).

    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)

  19. #2050474

    Ag brath ar an tsubstaint ghníomhach agus ar an mód gníomhaíochta, féadfaidh táirge íocshláinte tréidliachta nuatheiripe teacht faoi aon cheann de na trí chatagóir táirgí:

    Depending on the active substance and the mode of action, a novel therapy veterinary medicinal product could fall under any of the three product categories:

    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. #2061507

    Bunaithe ar na sonraí atá ar fáil agus ar an eolas reatha a ndearnadh achoimre air i gconclúid an Údaráis, níor tugadh faoi deara aon éifeachtaí díobhálacha a d’fhéadfadh a bheith bainteach le modh gníomhaíochta réabóra iontálaigh.

    Based on the available data and current knowledge summarised in the conclusion of the Authority no adverse effects that could be related to an endocrine disruptor mode of action were observed.

    Commission Implementing Regulation (EU) 2021/843 of 26 May 2021 renewing the approval of the active substance cyazofamid, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 (Text with EEA relevance)

  21. #2403359

    Tá na substaintí asóil grúpáilte toisc go bhfuil an modh gníomhaíochta céanna acu agus d’fhéadfadh sé go mbeadh éifeachtaí breiseáin acu freisin; is féidir anailís a dhéanamh orthu le chéile agus ba cheart leanúint leis sin a dhéanamh freisin.

    The azole substances are grouped because they have the same mode of action and could also have additive effects; they can and should also continue to be analysed together.

    Commission Implementing Decision (EU) 2022/1307 of 22 July 2022 establishing a watch list of substances for Union-wide monitoring in the field of water policy pursuant to Directive 2008/105/EC of the European Parliament and of the Council (notified under document C(2022) 5098) (Text with EEA relevance)

  22. #2403360

    Áirítear asocsastróibin mar aon le démhocsastróibin toisc go bhfuil an modh gníomhaíochta céanna aici; is féidir anailís a dhéanamh ar na substaintí sin le chéile agus ba cheart é sin a dhéanamh.

    Azoxystrobin is included alongside dimoxystrobin because it has the same mode of action; these substances can and should be analysed together.

    Commission Implementing Decision (EU) 2022/1307 of 22 July 2022 establishing a watch list of substances for Union-wide monitoring in the field of water policy pursuant to Directive 2008/105/EC of the European Parliament and of the Council (notified under document C(2022) 5098) (Text with EEA relevance)

  23. #2403362

    Tá na trí oibreán scéithe gréine grúpáilte toisc go bhfuil an modh gníomhaíochta céanna acu agus d’fhéadfadh sé go mbeadh éifeachtaí breiseáin acu, is féidir anailís a dhéanamh orthu le chéile freisin agus ba cheart é sin a dhéanamh.

    The three sunscreen agents are grouped because they have the same mode of action and could have additive effects, they too can and should be analysed together.

    Commission Implementing Decision (EU) 2022/1307 of 22 July 2022 establishing a watch list of substances for Union-wide monitoring in the field of water policy pursuant to Directive 2008/105/EC of the European Parliament and of the Council (notified under document C(2022) 5098) (Text with EEA relevance)

  24. #2512177

    Leis an eolas eolaíoch atá ar fáil faoi láthair maidir le meitibilítí de tháirgeadh miocrorgánach is féidir tuiscint níos fearr a fháil ar an ról atá ag na meitibilítí sin i modh gníomhaíochta na miocrorgánach a tháirgeann iad.

    The currently available scientific knowledge concerning metabolites produced by micro-organisms allows for a better understanding of the role those metabolites play in the mode of action of micro-organisms producing them.

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)

  25. #2513651

    gach faisnéis ábhartha maidir leis an tsubstaint ghníomhach dá bhforáiltear san Iarscríbhinn a ghabhann le Rialachán (AE) Uimh. 283/2013, lena n-áirítear an modh gníomhaíochta, galbhrú, so-ghalaitheacht agus tuaslagthacht an uisce.

    all relevant information on the active substance as provided for in of the Annex to Regulation (EU) No 283/2013, including mode of action, vapour pressure, volatility and water solubility.

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  26. #2513793

    modh gníomhaíocht (e.g. gníomhaíocht rialála fáis feithidí);

    mode of action (e. g. insect growth regulating activity);

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  27. #2514002

    Go háirithe, déanfaidh na Ballstáit meastóireacht ar an ról a bheadh ag ionfhabhtaíocht, pataigineacht, tocsaineacht agus gníomhaíocht mhiocróbach ábhartha fhéideartha sa mhodh gníomhaíochta in aghaidh an spriocorgánaigh.

    In particular, Member States shall evaluate the role of possible infectivity, pathogenicity, toxicity and relevant antimicrobial activity in the mode of action against the target organism.

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  28. #2514003

    Más infheidhme, tabharfar tuairisc ar fhachtóirí a chuireann le pataigineacht/nimhneacht miocrorgánaigh agus ar fhachtóirí comhshaoil a dhéanann difear do mhodh gníomhaíochta pataigineach.

    If applicable, factors that enhance the pathogenicity/virulence of a micro-organism and environmental factors affecting a pathogenic mode of action shall be described.

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  29. #2514004

    D’fhéadfadh faisnéis maidir leis an modh gníomhaíochta a bheith ina huirlis an-luachmhar chun rioscaí féideartha agus cuspóir an mhiocrorgánaigh sa táirge cosanta plandaí a shainaithint.

    Information on the mode of action can be a very valuable tool in identifying potential risks and purpose of the micro-organism in the plant protection product.

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  30. #2514048

    gach faisnéis ábhartha maidir leis an miocrorgánach, lena n-áirítear airíonna bitheolaíocha e.g. modh gníomhaíochta, marthanas, sainiúlacht an raoin óstaigh.

    all relevant information on the micro-organism, including biological properties e.g. mode of action, survival, host range specificity.

    Commission Regulation (EU) 2022/1441 of 31 August 2022 amending Regulation (EU) No 546/2011 as regards specific uniform principles for evaluation and authorisation of plant protection products containing micro-organisms (Text with EEA relevance)

  31. #2567626

    I gcás inmhíolú leanúnach, chun an riosca frithsheasmhachta a íoslaghdú, úsáid táirgí difriúla ina bhfuil substaintí gníomhacha éagsúla.

    In the case of continuous infestation; to minimise the risk of resistance, alternative products containing active substances with different mode of action should be used.

    Commission Implementing Regulation (EU) 2022/2330 of 28 November 2022 granting a Union authorisation for the single biocidal product 'Christiansen LD Bednet' in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)

  32. #3042610

    Ní mór úsáid an táirge seo a mhalartú le húsáid táirgí atá bunaithe ar shubstaintí gníomhacha eile a bhfuil modh gníomhaíochta difriúil acu chun frithsheasmhacht a sheachaint.

    The use of this product must be alternated with the use of products based on other active substances with different mode of action to avoid development of resistance.

    Commission Implementing Regulation (EU) 2023/2649 of 28 November 2023 granting a Union authorisation for the single biocidal product Hokoex in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

  33. #284826

    (4) De réir Threoir 2001/83/CE agus de réir na dTreoracha maidir le Feistí Leighis, is é príomh-mhodh gníomhaithe an táirge comhcheangail an bunús ar a gcinntear an réimeas rialúcháin is infheidhme maidir le comhcheangail de tháirgí íocshláinte agus d’fheistí leighis.

    (4) According to Directive 2001/83/EC and the Medical Device Directives the basis for deciding which regulatory regime is applicable to combinations of medicinal products and medical devices is the principal mode of action of the combination product.

    Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004

  34. #284828

    I gcás na dtáirgí sin, beag beann ar ról an fheiste leighis, ba cheart a mheas gurb é gníomh cógaseolaíoch, imdhíoneolaíoch nó meitibileach na gceall sin nó na bhfíochán sin príomh-mhodh gníomhaíochta an táirge comhcheangail.

    For these products, whatever the role of the medical device, the pharmacological, immunological or metabolic action of these cells or tissues should be considered to be the principal mode of action of the combination product.

    Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004

  35. #284919

    2. I gcás ina mbeidh cealla nó fíocháin inmharthana i dtáirge, measfar gurb iad gníomhaíocht chógaseolaíoch, imdhíoneolaíoch nó meitibileach na gceall nó na bhfíochán sin modh príomhúil gníomhaíochta an táirge.

    2. Where a product contains viable cells or tissues, the pharmacological, immunological or metabolic action of those cells or tissues shall be considered as the principal mode of action of the product.

    Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004

  36. #294002

    3.7.2.3.2. D'fhéadfadh staidéir thocsainchinéiteacha in ainmhithe agus i ndaoine, torthaí staidéir maidir le suíomh gníomhaíochta agus torthaí staidéir maidir le meicníocht nó modh gníomhaíochta faisnéis ábhartha a sholáthar a laghdaíonn nó a mhéadaíonn an imní faoi ghuaiseacha do shláinte an duine.

    3.7.2.3.2. Toxicokinetic studies in animals and humans, site of action and mechanism or mode of action study results may provide relevant information which reduces or increases concerns about the hazard to human health.

    Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006

  37. #294003

    Má thaispeántar go cinntitheach nach bhfuil baint ar bith ag an meicníocht nó modh gníomhaíochta atá sainaitheanta go soiléir le daoine nó nuair a bhíonn na difríochtaí tocsainchinéiteacha chomh mór sin gur cinnte nach mbeidh an t-airí guaiseach i ndaoine, ansin níor chóir substaint a chothaíonn éifeacht dhíobhálach ar atáirgeadh in ainmhithe turgnamhacha a aicmiú.

    If it is conclusively demonstrated that the clearly identified mechanism or mode of action has no relevance for humans or when the toxicokinetic differences are so marked that it is certain that the hazardous property will not be expressed in humans then a substance which produces an adverse effect on reproduction in experimental animals should not be classified.

    Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006

  38. #294067

    Más féidir a thaispeáint go cinntitheach, áfach, nach bhfuil baint ar bith ag an meicníocht nó modh gníomhaíochta atá sainaitheanta go soiléir le daoine nó nuair atá na difríochtaí tocsainchinéiteacha chomh mór sin gur cinnte nach mbeidh an t-airí guaiseach i ndaoine ansin ní aicmeofar substaint a chothaíonn éifeacht dhíobhálach ar atáirgeadh in ainmhithe turgnamhacha.

    However, if it can be conclusively demonstrated that the clearly identified mechanism or mode of action has no relevance for humans or when the toxicokinetic differences are so marked that it is certain that the hazardous property will not be expressed in humans then a substance which produces an adverse effect on reproduction in experimental animals shall not be classified.

    Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006

  39. #744656

    Na feistí ionracha ar fad i ndáil le hoscailtí colainne, seachas feistí máinliachta ionraí, a beartaíodh le haghaidh táirgí íocshláinte a thabhairt trí ionanálú, aicmítear mar aicme IIa iad, ach amháin má bhíonn tionchar bunriachtanach ag a modh gníomhaíochta ar éifeachtúlacht agus ar shábháilteacht na dtáirgí íocshláinte a thugtar agus iad sin a beartaíodh chun riochtaí lena ngabhann baol don bheatha a chóireáil, agus sa chás sin aicmítear mar aicme IIb iad.

    All invasive devices with respect to body orifices, other than surgically invasive devices, which are intended to administer medicinal products by inhalation are classified as class IIa, unless their mode of action has an essential impact on the efficacy and safety of the administered medicinal product or they are intended to treat life-threatening conditions, in which case they are classified as class IIb.

    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. )

  40. #1732415

    Shainaithin SCOEL an fhéidearthacht go dtarlódh ionsúchán suntasach tríd an gcraiceann i gcás déchlóiríd eitiléine agus chomhaontaigh ACSH teorainnluach praiticiúil, ar bhonn na faisnéise atá ar fáil, lena n-áirítear sonraí eolaíocha agus teicniúla, agus béim á leagan aige ar an easpa sonraí eolaíocha iontaofa cothrom le dáta atá ann, go háirithe sa mhéid a bhaineann le modh gníomhaíochta.

    SCOEL identified for ethylene dichloride the possibility of significant uptake through the skin and the ACSH agreed on a practical limit value, on the basis of the available information, including scientific and technical data, while stressing the lack of robust and up-to-date scientific data, especially concerning the mode of action.

    Directive (EU) 2019/130 of the European Parliament and of the Council of 16 January 2019 amending Directive 2004/37/EC on the protection of workers from the risks related to exposure to carcinogens or mutagens at work (Text with EEA relevance.)

  41. #1759114

    Agus measúnú IARC á chur san áireamh aige, tháinig SCOEL ar an gconclúid, i gcomhréir lena mhodheolaíocht, gur de ghrúpa carcanaigineach (A) “olaí mianracha mar olaí innill spíonta”, gan tairseach a lua a suíodh le modh gníomhaíochta 14.

    Taking into consideration the IARC assessment, SCOEL, in accordance with its methodology, concluded that "mineral oils as used engine oils" are carcinogenic group A with no indication for a mode of action-based threshold 14.

    Proposal for a DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Directive 2004/37/EC on the protection of workers from the risks related to exposure to carcinogens or mutagens at work

  42. #1805819

    Is le modh gníomhaíochta an táirge AE, le tiúchan coibhneasta a ábhair éagsúla, nó le haon pharaiméadar ábhartha eile a thacófar leis an maíomh go gcomhlíonann táirge leasacháin, i ndáil leis an PFC ábhartha, an fheidhm a leagtar síos san Iarscríbhinn seo.

    The claim that an EU fertilising product complies with the function set out in this Annex for the relevant PFC shall be supported by the product’s mode of action, the relative content of its various components, or any other relevant parameter.

    Regulation (EU) 2019/1009 of the European Parliament and of the Council of 5 June 2019 laying down rules on the making available on the market of EU fertilising products and amending Regulations (EC) No 1069/2009 and (EC) No 1107/2009 and repealing Regulation (EC) No 2003/2003 (Text with EEA relevance)

  43. #2050488

    Cuimsítear leis na tosca riosca is féidir a bhreithniú bunús an ábhair tosaigh (cealla etc.), an mód gníomhaíochta san ainmhí (iomadú, tosú ar fhreagairt imdhíonachta, buaine sa chorp, etc.), leibhéal ionramhála ceall (mar shampla, an modh monaraíochta), cónascadh na substainte gníomhaí le móilíní bithghníomhacha nó ábhair struchtúracha, fairsinge na hinniúlachta macasamhlúcháin de víris nó de mhiocrorgánaigh a úsáidtear in vivo, leibhéal comhtháthaithe seicheamh aigéad núicléasach nó géinte sa ghéanóm, an fheidhmiúlacht fhadama, an riosca oncaigéineach, na héifeachtaí nár bhain an sprioc amach, agus an mód tabhartha nó úsáide.

    Risk factors that may be considered include the origin of the starting material (cells etc.), the mode of action in the animal (proliferation, initiation of an immune response, permanence in the body, etc.), the level of cell manipulation (for example, the manufacturing process), the combination of the active substance with bioactive molecules or structural materials, the extent of replication competence of viruses or micro-organisms used in vivo, the level of integration of nucleic acids sequences or genes into the genome, the long-time functionality, the risk of oncogenicity, the off-target effects and the mode of administration or use.

    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)

  44. #2227806

    Ós rud é go bhfuil substaint ghníomhach sa táirge, agus go bhfuil an táirge ceaptha le héifeacht um shrianadh a imirt ar orgánach díobhálach trí mhodh gníomhaíochta nach bhfuil fisiciúil ná meicniúil amháin, ba cheart an táirge a mheas mar tháirge bithicídeach mar a shainítear in Airteagal 3(1), pointe (a), de Rialachán (AE) Uimh. 528/2012).

    Given that the product contains an active substance and is intended to exert a controlling effect on a harmful organism by a mode of action that is not merely physical or mechanical, the product should be considered a biocidal product as defined in Article 3(1), point (a), of Regulation (EU) No 528/2012.

    Commission Implementing Decision (EU) 2022/146 of 1 February 2022 determining whether a product containing Alkyl (C12-16) dimethylbenzyl ammonium chloride is a biocidal product, pursuant to Article 3(3) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)

  45. #2340930

    I dtaca le tástálacha ar éisc maidir le tocsaineacht ghearrthéarmach i staid an tsutha agus i staid an ghilidín saic (OECD TG 212), ar cuireadh tús leo roimh an 14 Aibreán 2022 [OP, cuir isteach dáta theacht i bhfeidhm an Rialacháin leasaithigh], measfar iad a bheith iomchuí chun an ceanglas sin maidir le faisnéis a chomhlíonadh ar choinníoll nach an-lipifíleach an tsubstaint (loga Kow > 4) ná nach léirítear airí suaite inchríneach ná aon modh gníomhaíochta sonrach eile.”

    Fish short-term toxicity tests on embryo and sac-fry stages (OECD TG 212) that were initiated before 14 April 2022 shall be considered appropriate to address this standard information requirement provided that the substance is not highly lipophilic (log Kow > 4) or there is no indication of endocrine disrupting properties or any other specific mode of action.’;

    Commission Regulation (EU) 2022/477 of 24 March 2022 amending Annexes VI to X to Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) (Text with EEA relevance)

  46. #2409501

    Ós rud é go bhfuil substaint ghníomhach sa táirge agus go bhfuil an táirge ceaptha le horgánaigh dhíobhálacha a dhíspreagadh trí mhodh gníomhaíochta nach bhfuil fisiciúil ná meicniúil amháin, ba cheart an táirge a mheas mar tháirge bithicídeach faoi mar a shainmhínítear in Airteagal 3(1), pointe (a), de Rialachán (AE) Uimh. 528/2012.

    Given that the product contains an active substance and is intended to deter harmful organism by a mode of action that is not merely physical or mechanical, the product should be considered a biocidal product as defined in Article 3(1), point (a), of Regulation (EU) No 528/2012.

    Commission Implementing Decision (EU) 2022/1497 of 8 September 2022 determining whether a product containing ‘Capsicum oleoresin expeller pressed’ is a biocidal product, pursuant to Article 3(3) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)

  47. #2512178

    Ag cur san áireamh gur substaintí ceimiceacha iad meitibilítí de tháirgeadh miocrorgánach, d’fhéadfadh an méid a d’fhéadfadh siad cur leis an modh gníomhaíochta a bheith ina chúis le héiginnteacht dhlíthiúil maidir le cé acu is gá nó nach gá na ceanglais dá bhforáiltear i gCuid A den Iarscríbhinn sin maidir le substaintí gníomhacha ceimiceacha, nó i gCuid B de, maidir le miocrorgánaigh, a chomhlíonadh leis na hiarratais sin.

    Taking into consideration that metabolites produced by micro-organisms are chemical substances, their possible contribution to the mode of action may lead to legal uncertainty on whether applications are to comply with the requirements provided for in Part A of that Annex concerning chemical active substances, or in Part B thereof, concerning micro-organisms.

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)

  48. #2512182

    Le staid reatha an eolais eolaíoch maidir le miocrorgánaigh, is féidir cur chuige níos fearr agus níos sonraí a ghlacadh i leith measúnú a dhéanamh orthu, rud atá bunaithe ar an modh gníomhaíochta atá acu agus ar shaintréithe na speiceas faoi seach agus, i gcás inarb infheidhme, na dtréithchineál miocrorgánach faoi seach.

    The current state of scientific knowledge on micro-organisms allows for a better and more specific approach for their assessment, which is based on their mode of action and the ecological characteristics of the respective species and, where applicable, the respective strains of micro-organisms.

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)

  49. #2512493

    I gcás modh gníomhaíochta pataiginigh nó seadánaigh ar an spriocorgánach, tabharfar faisnéis maidir le láthair an ionfhabhtaithe agus an modh iontrála isteach sa spriocorgánach, an dáileog ionfhabhtaíoch agus céimeanna soghabhálacha an spriocorgánaigh.

    In case of a pathogenic or parasitic mode of action on the target organism, information on the site of infection and mode of entry into the target organism, the infective dose and the susceptible stages of the target organism shall be given.

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)

  50. #2512746

    Má bhíonn gá le staidéir phataigineachta/ionfhabhaíochta le haghaidh aon cheann de na grúpaí orgánach nach spriocorgánaigh iad a shonraítear i bpointí 8.1 go 8.6, beidh an rogha maidir le speiceas iomchuí an ghrúpa orgánach nach spriocorgánaigh iad sin bunaithe ar airíonna bitheolaíocha an mhiocrorgánaigh (lena n-áirítear sonraíocht an raoin óstaigh, an modh gníomhaíochta agus an éiceolaíocht), ar na patrúin úsáide atá beartaithe don táirge cosanta plandaí (e.g. barraí cóireáilte, minicíocht, amchláir, patrúin úsáide amhail spraeáil nó scuabadh) agus tabharfar aird ar threoirlínte ábhartha, i gcás ina bhfuil a leithéid ar fáil.

    If pathogenicity/infectivity studies are required for any of the non-target organism groups indicated in points 8.1 to 8.6, the choice of the appropriate species of that non-target organisms group shall be based on the biological properties of the micro-organism (including the host range specificity, mode of action and ecology), the proposed use pattern(s) of the plant protection product (e.g. treated crops, frequency, timings, use patterns such as spraying or brushing) and consider relevant guidelines, where available.

    Commission Regulation (EU) 2022/1439 of 31 August 2022 amending Regulation (EU) No 283/2013 as regards the information to be submitted for active substances and the specific data requirements for micro-organisms (Text with EEA relevance)