Gaois

Cóip statach de shonraí a easpórtáiltear ó IATE ó am go chéile atá sa chnuasach seo. Níor cheart glacadh leis gurb ionann i gcónaí an t-eolas a thugtar faoi iontráil anseo agus a bhfuil sa leagan reatha den iontráil ar IATE. Is féidir an leagan reatha sin a cheadú ach cliceáil ar an nasc atá ar thaobh na láimhe deise ag barr gach iontrála. Breis eolais »

3 thoradh

  1. SCIENCE|natural and applied sciences|applied sciences

    #639543

    IATE #2232766
    bailíochtú modha Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Sa tuairim eolaíoch uaidh, mheas an tÚdarás nach bhféadfadh sé teacht ar a chonclúidí maidir le sábháilteacht 3-FL gan na staidéir agus na sonraí eolaíocha ar bhailíochtú modha MS, NMR agus HPAEC-PAD agus na torthaí maidir le haitheantas 3-FL agus na seachtháirgí carbaihiodráite atá sa bhia núíosach a chinneadh; an tuairisc ar thréithchineál táirgthe 3-FL géinmhodhnaithe; deimhniú deascaidh thréithchineál táirgthe ghéinmhodhnaithe 3-fúcaishiollachtóis...' Tagairt "Rialachán Cur Chun Feidhme (AE) 2023/52 lena n-údaraítear 3-Fúcaishiollachtós arna tháirgeadh le tréithchineál díorthach Escherichia coli BL21(DE3) a chur ar an margadh mar bhia núíosach agus lena leasaítear Rialachán Cur Chun Feidhme (AE) 2017/2470,CELEX:32023R0052/GA"
    Methodenvalidierung
    de
    method validation
    en
    Sainmhíniú process of establishing the performance characteristics and limitations of a method and the identification of the influences which may change these characteristics and to what extent Tagairt "FDA, Methods. 'Method Verification and Validation' (24.11.2022). Document Number: ORA-LAB.5.4.5. Revision #: 02 Revision Date: 06/30/2020"
  2. EUROPEAN UNION|EU institutions and European civil service|Community body · SOCIAL QUESTIONS|health|pharmaceutical industry · ENVIRONMENT · PRODUCTION, TECHNOLOGY AND RESEARCH|research and intellectual property|research

    #610263

    IATE #858001
    an Lárionad Eorpach um Bailíochtú Modhanna Malartacha Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Europäisches Zentrum zur Validierung alternativer Methoden | ECVAM | CEVMA
    de
    European Centre for the Validation of Alternative Methods | ECVAM
    en
    Centre européen pour la validation de méthodes alternatives | CEVMA | ECVAM
    fr
    Sainmhíniú """Le CEVMA a été créé par la Commission européenne dans les années 1990 pour coordonner le développement et la validation de méthodes alternatives à l'expérimentation animale. Ce centre, qui fait partie du Centre Commun de Recherche de l'Union européenne, organise régulièrement des ateliers et des task forces pour réexaminer le statut actuel des tests alternatifs et pour fournir des conseils sur la promotion de l'intégration de tests in vitro et d'autres méthodes dans le processus de réglementation. À l’heure actuelle, trois méthodes alternatives ont reçu l'agrément du CEVMA et dix autres sont en voie de l'obtenir.""" Tagairt "Commission, DG Recherche < http://ec.europa.eu/research/leaflets/animal/page_65_fr.html > (27/09/2006)"
  3. SOCIAL QUESTIONS|health|medical science

    #637889

    IATE #1909235
    an Coiste Comhordúcháin Idirghníomhaireachta um Bailíochtú Modhanna Malartacha Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    ICCVAM | Interagency Coordinating Committee on the Validation of Alternative Methods
    en
    Sainmhíniú permanent committee of the NIEHS under the National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM) Tagairt "U.S. Department of Health and Human Services. National Toxicology Program. About ICCVAM, http://ntp.niehs.nih.gov/pubhealth/evalatm/iccvam/index.html [17.10.2014]"
    Nóta ICCVAM is composed of representatives from 15 U.S. Federal regulatory and research agencies that require, use, generate or disseminate toxicological and safety testing information