Gaois

Search direction

Search mode

Filter results

Collections

10 results in 7 documents

  1. #1736428

    Is féidir sonraí cobhsaíochta ó na stoic hoiméapatacha a aistriú go caoluithe nó go neartchaoluithe a rinneadh as na stoic sin.

    Stability data from the homeopathic stocks are generally transferable to dilutions/potentisations obtained thereof.

    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. #2050652

    Is féidir sonraí cobhsaíochta ó na stoic hoiméapatacha a aistriú go caoluithe nó go neartchaoluithe a rinneadh as na stoic sin.

    Stability data from the homeopathic stocks are generally transferable to dilutions/potentisations obtained thereof.

    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)

  3. #3203292

    Is féidir caoluithe comhréireacha a dhéanamh do chainníochtaí eile, más mian leo.

    Proportional dilutions can be made for other quantities, if desired.

    Commission Implementing Regulation (EU) 2024/267 of 17 January 2024 granting a Union authorisation for the single biocidal product DEC-SPORE 200 Plus in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

  4. #587102

    Ina theannta sin, le linn méid a shocrú don leibhéal feabhsúcháin is gá, déanfaidh an clár athbhreithniú ar roinnt blianta d'fhaisnéis stairiúil, lena n-áirítear caillteanais, ciontóireacht, caoluithe, agus ráta láimhdeachais earraí infhaighte;

    In addition, in sizing the required enhancement level, the program shall review several years of historical information, including losses, delinquencies, dilutions, and the turnover rate of the receivables;

    Regulation (EU) No 575/2013 of the European Parliament and of the Council of 26 June 2013 on prudential requirements for credit institutions and investment firms and amending Regulation (EU) No 648/2012 Text with EEA relevance

  5. #1677164

    déantar méid an leibhéil fheabhsaithe is gá sa chlár ABCP a ríomh trí aird a thabhairt ar roinnt blianta d’fhaisnéis stairiúil, lena n-áirítear caillteanais, ciontóireacht, caoluithe, agus ráta láimhdeachais earraí infhaighte;

    the size of the required enhancement level in the ABCP programme is calculated taking into account several years of historical information, including losses, delinquencies, dilutions, and the turnover rate of the receivables;

    Regulation (EU) 2017/2401 of the European Parliament and of the Council of 12 December 2017 amending Regulation (EU) No 575/2013 on prudential requirements for credit institutions and investment firms

  6. #2012267

    Sa mheasúnú foriomlán seo, tabharfaidh na Ballstáit aird ar leith ar na treoracha lipéadaithe riachtanacha maidir le bearta i ndáil le cúradh agus cobhsaíocht chaolúcháin an fhoirmlithe.

    In this overall assessment, Member States shall pay particular attention to the necessary labelling instructions concerning the measures to address foaming and stability of dilutions of the formulation.

    Commission Implementing Regulation (EU) 2021/567 of 6 April 2021 approving the low-risk active substance aqueous extract from the germinated seeds of sweet Lupinus albus 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 Commission Implementing Regulation (EU) No 540/2011 (Text with EEA relevance)

  7. #293555

    Nuair a dhéantar breathnuithe ar ghreannú/creimeadh craicinn i staidéir ghéarthocsaineachta, suas tríd an dáileog theorann, níl tástáil bhreise riachtanach, ar choinníoll go mbíonn na caoluithe a úsáidtear agus na speicis a thástáltar coibhéiseach.

    When observations are made of skin irritation/corrosion in acute toxicity studies and are observed up through the limit dose, additional testing is not needed, provided that the dilutions used and species tested are equivalent.

    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

  8. #586008

    áiritheoidh an institiúid go bhfaighidh sí tuarascálacha tráthúla mionsonraithe a ndóthain ón seirbhíseoir ar aosú agus ar chaolú na n-earraí infhaighte lena áirithiú go gcomhlíonfar critéir incháilitheachta na hinstitiúide agus na beartais airleacain a rialaíonn na hearraí infhaighte ceannaithe, agus le modh éifeachtach a chur ar fáil le faireachán a dhéanamh ar théarmaí díolta agus caolúcháin an díoltóra agus iad sin a dhaingniú.

    the institution shall ensure that it receives from the servicer timely and sufficiently detailed reports of receivables ageings and dilutions to ensure compliance with the institution's eligibility criteria and advancing policies governing purchased receivables, and provide an effective means with which to monitor and confirm the seller's terms of sale and dilution.

    Regulation (EU) No 575/2013 of the European Parliament and of the Council of 26 June 2013 on prudential requirements for credit institutions and investment firms and amending Regulation (EU) No 648/2012 Text with EEA relevance

  9. #1736420

    Má bhaineann caoluithe leis an bpróiseas, tabharfar na céimeanna caolaithe sin i gcomhréir leis na modhanna monaraíochta hoiméapatacha atá leagtha síos sa mhonagraf ábhartha de Pharmacopoeia Eorpach nó, ina éagmais sin, in pharmacopoeia oifigiúil de chuid Ballstáit.

    In case dilutions are involved, these dilution steps shall be done in accordance with the homeopathic manufacturing methods laid down in the relevant monograph of the European Pharmacopoeia or, in absence thereof, in an official pharmacopoeia of a Member State.

    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)

  10. #2050645

    I gcás ina mbaineann caoluithe leis an bpróiseas, déanfar na céimeanna caolaithe sin i gcomhréir leis na modhanna monaraíochta hoiméapatacha a leagtar síos sa mhonagraf ábhartha de Pharmacopoeia Eorpach nó, ina éagmais sin, in pharmacopoeia oifigiúil Ballstáit.

    Where dilutions are involved, those dilution steps shall be done in accordance with the homeopathic manufacturing methods laid down in the relevant monograph of the European Pharmacopoeia or, in absence thereof, in an official pharmacopoeia of a Member State.

    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)