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16 toradh

  1. EUROPEAN UNION|European Union law|EU act|regulation (EU)
    an Rialachán maidir le feistí leighis diagnóiseacha in vitro Tagairt "Rialachán (AE) 2017/746 maidir le feistí leighis diagnóiseacha in vitro agus lena n-aisghairtear Treoir 98/79/CE agus Cinneadh 2010/227/AE ón gCoimisiún,CELEX:32017R0746/GA Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    Rialachán IVD Tagairt "Togra le haghaidh Rialachán lena leasaítear Rialachán (AE) 2017/746 a mhéid a bhaineann le forálacha idirthréimhseacha le haghaidh feistí leighis diagnóiseacha in vitro áirithe agus le haghaidh chur i bhfeidhm iarchurtha na gceanglas maidir le feistí intí,CELEX:52021PC0627/GA Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    Verordnung über In-vitro-Diagnostika | Verordnung (EU) 2017/746 des Europäischen Parlaments und des Rates vom 5. April 2017 über In-vitro-Diagnostika und zur Aufhebung der Richtlinie 98/79/EG und des Beschlusses 2010/227/EU der Kommission | IVD-Verordnung
    de
    Sainmhíniú Verordnung, mit der die Regeln für das Inverkehrbringen, die Bereitstellung auf dem Markt und die Inbetriebnahme von für den menschlichen Gebrauch bestimmten In-vitro-Diagnostika und deren Zubehör in der Union festgelegt werden Tagairt "Verordnung (EU) 2017/746 des Europäischen Parlaments und des Rates vom 5. April 2017 über In-vitro-Diagnostika und zur Aufhebung der Richtlinie 98/79/EG und des Beschlusses 2010/227/EU der Kommission (Text von Bedeutung für den EWR. )"
    In Vitro Diagnostic Medical Devices Regulation | Regulation (EU) 2017/746 on in vitro diagnostic medical devices | IVDR | In Vitro Diagnostic Regulation
    en
    Sainmhíniú regulation which aims to ensure the smooth functioning of the internal market as regards in vitro diagnostic medical devices, taking as a base a high level of protection of health for patients and users, and taking into account the small and medium-sized enterprises that are active in this sector Tagairt "COM-EN, based on:Regulation (EU) 2017/746 on in vitro diagnostic medical devices"
    règlement relatif aux dispositifs médicaux de diagnostic in vitro
    fr
    Sainmhíniú règlement visant à garantir le bon fonctionnement du marché intérieur des dispositifs médicaux de diagnostic in vitro, sur la base d'un niveau élevé de protection de la santé pour les patients et les utilisateurs, et fixant des normes élevées de qualité et de sécurité des dispositifs médicaux de diagnostic in vitro afin de faire face aux enjeux communs de sécurité relatifs à ces produits Tagairt "COM-FR, d'après le règlement (UE) 2017/746 du Parlement européen et du Conseil relatif aux dispositifs médicaux de diagnostic in vitro et abrogeant la directive 98/79/CE et la décision 2010/227/UE de la Commission"
  2. EDUCATION AND COMMUNICATIONS|information technology and data processing|data processing|database · SOCIAL QUESTIONS|health|health policy|organisation of health care|medical device · SOCIAL QUESTIONS|health|illness|epidemic
    Bunachar Sonraí maidir le Modhanna Tástála agus Feistí Diagnóiseacha In Vitro COVID-19 Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    COVID-19 In Vitro Diagnostic Devices and Test Methods Database
    en
    Sainmhíniú database curated and periodically updated by the JRC whose objective is to collect in a single place all publicly available information on performance of CE-marked in vitro diagnostic medical devices (IVDs) as well as laboratory-developed devices and related test methods for COVID-19 Tagairt "COM-Terminology Coordination, based on: European Commission. JRC. 'COVID-19 In Vitro Diagnostic Devices and Test Methods Database' (16.6.2021)"
  3. SOCIAL QUESTIONS|health · PRODUCTION, TECHNOLOGY AND RESEARCH|technology and technical regulations
    feiste leighis dhiagnóiseach in vitro Tagairt "Rialachán (AE) 2017/746 maidir le feistí leighis diagnóiseacha in vitro agus lena n-aisghairtear Treoir 98/79/CE agus Cinneadh 2010/227/AE ón gCoimisiún"
    ga
    Sainmhíniú aon fheiste leighis ar imoibrí, táirge imoibrithe, calabróir, ábhar rialaithe, fearas, uirlis, gaireas, píosa trealaimh, bogearraí nó córas í, a úsáidtear ina haonar nó i gcomhcheangal le rud eile agus atá beartaithe a úsáid in vitro ag an monaróir chun eiseamail a scrúdú, lena n-áirítear deonú fola agus fíochán, arna ndíorthú ó chorp an duine, go heisiach nó go príomha chun faisnéis maidir le haon cheann amháin nó níos mó díobh seo a leanas a sholáthar: (a) a bhaineann le próiseas nó le staid fhiseolaíoch nó phaiteolaíoch; (b) a bhaineann le lagú fisiciúil mó meabhrach ó bhroinn; (c) a bhaineann le togracht chun reachta sláinte nó chun galair; (d) chun an tsábháilteacht agus an oiriúnacht d'fhaighteoirí féideartha a chinneadh; (e) chun an fhreagairt ar chóireáil nó frithghníomhartha i gcoinne cóireála a thuar; (f) chun bearta teiripeacha a shainmhíniú nó chun faireachán a dhéanamh orthu Tagairt "Rialachán (AE) 2017/746 maidir le feistí leighis diagnóiseacha in vitro agus lena n-aisghairtear Treoir 98/79/CE agus Cinneadh 2010/227/AE ón gCoimisiún"
    In-vitro-Diagnostikum | Produkt für die In-vitro-Diagnose
    de
    Sainmhíniú "Medizinprodukt IATE:1442463 , das als Reagenz, Reagenzprodukt, Kalibrator, Kontrollmaterial, Kit, Instrument, Apparat, Gerät, Software oder System vom Hersteller zur In-vitro-Untersuchung von aus dem menschlichen Körper stammenden Proben bestimmt ist und dazu dient, Informationen zu liefern a) über physiologische oder pathologische Prozesse oder Zustände, b) über kongenitale körperliche oder geistige Beeinträchtigungen, c) über die Prädisposition für einen bestimmten gesundheitlichen Zustand oder eine bestimmte Krankheit, d) zur Feststellung der Unbedenklichkeit und Verträglichkeit bei den potenziellen Empfängern, e) über die voraussichtliche Wirkung einer Behandlung oder die voraussichtlichen Reaktionen darauf oder f) zur Festlegung oder Überwachung therapeutischer Maßnahmen" Tagairt "vgl. Verordnung (EU) 2017/746 über In-vitro-Diagnostika, Art.2 Abs.2 CELEX:32017R0746/DE"
    in vitro diagnostic medical device | IVD medical device | IVD | device used for in vitro diagnosis
    en
    Sainmhíniú "any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, piece of equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information on one or more of the following: - concerning a physiological or pathological process or state; - concerning congenital physical or mental impairments; - concerning the predisposition to a medical condition or a disease; - to determine the safety and compatibility with potential recipients; - to predict treatment response or reactions; - to define or monitoring therapeutic measures." Tagairt "Article 2(2) of Regulation (EU) 2017/746 on in vitro diagnostic medical devices"
    Nóta "Specimen receptacles are also deemed to be in vitro diagnostic medical devices."
    dispositif médical de diagnostic in vitro | dispositif destiné au diagnostic in vitro
    fr
    Sainmhíniú "tout dispositif médical qui consiste en un réactif, un produit réactif, un matériau d'étalonnage, un matériau de contrôle, une trousse, un instrument, un appareil, un équipement, un logiciel ou un système, utilisé seul ou en association, destiné par le fabricant à être utilisé in vitro dans l'examen d'échantillons provenant du corps humain, y compris les dons de sang et de tissus, uniquement ou principalement dans le but de fournir des informations sur un ou plusieurs des éléments suivants: - concernant un processus ou état physiologique ou pathologique; - concernant des déficiences congénitales physiques ou mentales; - concernant la prédisposition à une affection ou à une maladie; - permettant de déterminer si un traitement donné est sûr pour des receveurs potentiels et compatible avec eux; - permettant de prévoir la réponse ou les réactions à un traitement; - permettant de définir ou de contrôler des mesures thérapeutiques" Tagairt "Règlement (UE) 2017/746 relatif aux dispositifs médicaux de diagnostic in vitro"
    Nóta Les récipients pour échantillons sont également réputés être des dispositifs médicaux de diagnostic in vitro.
  4. SOCIAL QUESTIONS|health|medical science
    scór greannachais in vitro Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    in vitro irritancy score | IVIS
    en
    Sainmhíniú an empirically-derived formula used in the Bovine Corneal Opacity and Permeability (BCOP) assay whereby the mean opacity and mean permeability values for each treatment group are combined into a single in vitro score for each treatment group Tagairt "Commission Regulation (EU) No 1152/2010 amending Regulation (EC) No 440/2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) CELEX:32010R1152/EN"
    Nóta The IVIS = mean opacity value + (15 × mean permeability value).
  5. SOCIAL QUESTIONS|health|medical science
    scrúdú fótatocsaineachta 3T3 NRU in vitro Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    in vitro 3T3 NRU phototoxicity test
    en
    Sainmhíniú test used to identify the phototoxic potential of a test substance induced by the excited chemical after exposure to light. The test evaluates photo-cytotoxicity by the relative reduction inviability of cells exposed to the chemical in the presence versus absence of light. Substances identified by this test are likely to be phototoxic in vivo following systemic application and distribution to the skin, or after topical application Tagairt "Council Regulation (EC) No 440/2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) CELEX:32008R0440/EN"
    test de phototoxicité in vitro 3T3 NRU
    fr
  6. SOCIAL QUESTIONS|health|medical science · SCIENCE|natural and applied sciences|life sciences
    tástáil in vitro ar mhalartú comhchrómaitide Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    In-vitro-Schwesterchromatidaustausch-Test | Schwesterchromatidaustausch-Test | SCE-Test
    de
    Sainmhíniú zytogenetisches Testsystem, das Schwesterchromatidaustauschvorgänge aufzeigen kann Tagairt "Leila Violette Khubnazar: „DNA-Strangbrüche in humanen HL-60 Promyelozytenleukämiezellen zur Einschätzung biologischer Wirkungen nach Exposition mit hochfrequenten elektromagnetischen Feldern (2450 MHz)“ [Dissertation]. Berlin: 2006, http://www.diss.fu-berlin.de/diss/servlets/MCRFileNodeServlet/FUDISS_derivate_000000014247/DoktoratxKhubnazar.pdf (23.10.2017)"
    sister chromatid exchange assay in vitro | assays | sister chromatid exchange test | tests | SCE test | sister chromatid exchange assay | (SCE)
    en
    Sainmhíniú short-term test for the detection of reciprocal exchanges of DNA between two sister chromatids of a duplicating chromosome Tagairt "Council Regulation (EC) No 440/2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) CELEX:32008R0440/EN"
    essai in vitro d'échange de chromatides-soeurs | test d'échange des chromatides-soeurs | SCE | test d'échange des chromatides fraternelles
    fr
    Sainmhíniú Test à court terme destiné à déceler les échanges réciproques d'ADN entre deux chromatides-soeurs d'un chromosome se dédoublant Tagairt Directive 87/302/CEE de la Commission
  7. SOCIAL QUESTIONS|health|medical science|toxicology
    tástáil micreanúicléis in vitro i gcealla mamach Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    in vitro mammalian cell micronucleus test | MNvit assay | in vitro mouse micronucleus test
    en
    Sainmhíniú "genotoxicity test for the detection of micronuclei [ IATE:1033008 ] (MN) in the cytoplasm [ IATE:1077370 ] of interphase [ IATE:1530134 ] cells" Tagairt "OECD. Environment Directorate. Chemical Safety and Biosafety. Testing of Chemicals. In Vitro Mammalian Cell Micronucleus Test (MNvit) http://www.oecd.org/LongAbstract/0,3425,en_2649_34377_39780113_1_1_1_1,00.html [13.4.2012]"
    Nóta "Micronuclei [ IATE:1033008 ] may originate from acentric chromosome [ IATE:1507541 ] fragments (i.e. lacking a centromere [ IATE:1620877 ]), or whole chromosomes that are unable to migrate to the poles during the anaphase [ IATE:1502711 ] stage of cell division [ IATE:1544625 ]. The assay detects the activity of clastogenic [ IATE:1684795 ] and aneugenic chemicals [ IATE:1588368 ] (substances and mixtures) (1) (2) in cells that have undergone cell division during or after exposure to the test substance."
  8. SOCIAL QUESTIONS|health|medical science|toxicology
    tástáil shaobhadh crómasóim in vitro i mamaigh Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    In-vitro-Test auf Chromosomenaberrationen
    de
    in vitro mammalian chromosomal aberration test | in vitro chromosomal aberration test | in vitro mammalian cell chromosomal aberration test in human lymphocytes
    en
    Nóta "The test is described in OECD TG 473, In Vitro Mammalian Chromosome Aberration Test (1997) and in Council Regulation (EC) No 440/2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) CELEX:32008R0440/EN"
    Essai d'aberration chromosomique in vitro chez les mammifères
    fr
  9. SCIENCE|natural and applied sciences|life sciences
    tástáil sócháin gaiméite in vitro i mamaigh Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    In-vitro-Genmutationstest an Säugetierzellen
    de
    in vitro mammalian cell gene mutation test
    en
    Sainmhíniú mutation test which can be used to detect gene mutations induced by chemical substances Tagairt "COM-EN, based on:Commission Regulation (EC) No 440/2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) CELEX:32008R0440/EN"
    essai in vitro de mutation génique sur cellules de mammifères
    fr
  10. SOCIAL QUESTIONS|family|artificial reproduction · SOCIAL QUESTIONS|health|medical science · AGRICULTURE, FORESTRY AND FISHERIES|agricultural activity|livestock farming
    toirchiú <i>in vitro</i> Tagairt "Togra le haghaidh Rialachán maidir le caighdeáin cháilíochta agus sábháilteachta le haghaidh substaintí de bhunús daonna a bheartaítear lena n-úsáid sa duine agus lena n-aisghairtear Treoracha 2002/98/CE agus 2004/23/CE, CELEX:52022PC0338/GA Faomhadh an téarma seo mar chuid de Thionscadal Lex"
    ga
    Comhthéacs 'I rith 2012, bhí an IMB mar chathaoirleach ar an tascfhórsa Eorpach chun na treoirlínte ar an gcóras faireachais feistí leighis (MEDDEV 2.12-1) a leasú, a bhfuil feistí toirchithe in vitro/ teicneolaíochtaí atáirgthe cúnta go sonrach san áireamh ann laistigh de scóip an chórais fhaireachais mar aon le mionsonrú níos mó maidir le ceanglais tuairiscithe d’fheistí nach dtagann i dteagmháil le hothair de ghnáth.' Tagairt "'Tuarascáil Bhliantúil 2012 - an tSláinte Phoiblí agus Sláinte Ainmhithe,' Bord Leigheasra na hÉireann, https://www.hpra.ie/docs/default-source/publications-forms/corporate-policy-documents/tuarasc%C3%A1il-bhliant%C3%BAil-2012-imb.pdf?sfvrsn=2 [8.11.2022]"
    cóireáil IVF Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    IVF Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    in vitro fertilisation | IVF | fertilisation in vitro | in-vitro fertilisation
    en
    Sainmhíniú process by which egg cells are fertilised by sperm outside the body, in vitro Tagairt "Wikipedia > In vitro fertilisation (23.5.2022)"
    fertilisatio in vitro
    la
  11. PRODUCTION, TECHNOLOGY AND RESEARCH|technology and technical regulations|biotechnology
    tras-scríobh <i>in vitro</i> Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    in vitro-Transcription
    de
    Sainmhíniú Verfahren, bei dem mRNA zellfrei, d.h.unter Verwendung entsprechend aufbereiteter Zellextrakte, in vitro synthetisiert wird. Tagairt Ibelgaufts H.,Gentechnologie von A bis Z,VCH Verlag
    in vitro transcription
    en
    Sainmhíniú laboratory procedure that allows for template-directed synthesis of RNA molecules of any sequence from short oligonucleotides to those of several kilobases in μg to mg quantities based on engineering of a template that includes a bacteriophage promoter sequence (e.g. from the T7 coliphage) upstream of the sequence of interest followed by transcription using the corresponding RNA polymerase Tagairt "Beckert B., Masquida B. (2011) 'Synthesis of RNA by In Vitro Transcription' (3.3.2021). In: Nielsen H. (eds) RNA. Methods in Molecular Biology (Methods and Protocols), vol 703. Humana Press."
  12. SOCIAL QUESTIONS|health|health policy|organisation of health care|medical device
    diagnóisic chompánaigh Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    therapiebegleitendes Diagnostikum
    de
    Sainmhíniú Produkt, das für die sichere und wirksame Verwendung eines dazugehörigen Arzneimittels wesentlich ist, um | a) | Patienten vor und/oder während der Behandlung zu identifizieren, die mit der größten Wahrscheinlichkeit von dem dazugehörigen Arzneimittel profitieren, oder | b) | Patienten vor und/oder während der Behandlung zu identifizieren, bei denen wahrscheinlich ein erhöhtes Risiko von schwerwiegenden unerwünschten Reaktionen infolge einer Behandlung mit dem dazugehörigen Arzneimittel besteht Tagairt "Verordnung (EU) 2017/746 über In-vitro-Diagnostika und zur Aufhebung der Richtlinie 98/79/EG und des Beschlusses 2010/227/EU der Kommission, Art.2 Nr.7; ABl. L_117/2017, S.176 CELEX:32017R0746/DE"
    companion diagnostic | in vitro companion diagnostic device | IVD companion diagnostic device | CDx | companion diagnostics
    en
    Sainmhíniú device which is essential for the safe and effective use of a corresponding medicinal product to:(a)identify, before and/or during treatment, patients who are most likely to benefit from the corresponding medicinal product; or(b)identify, before and/or during treatment, patients likely to be at increased risk of serious adverse reactions as a result of treatment with the corresponding medicinal product. Tagairt "Regulation (EU) 2017/746 on in vitro diagnostic medical devices"
    diagnostic compagnon
    fr
    Sainmhíniú tout dispositif essentiel pour une utilisation sûre et efficace d'un médicament donné visant àa) identifier, avant et/ou pendant le traitement, les patients les plus susceptibles de bénéficier du médicament en question; oub) identifier, avant et/ou pendant le traitement, les patients susceptibles de présenter un risque accru d'effets indésirables graves en réaction au traitement par le médicament en question Tagairt "Règlement (UE) 2017/746 relatif aux dispositifs médicaux de diagnostic in vitro, article 2, point 7)"
  13. AGRICULTURE, FORESTRY AND FISHERIES|agricultural activity|crop production|plant propagation
    saothrán fíocháin Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs '... bia atá déanta de shaothrán cille nó saothrán fíocháin a dhíorthaítear ó ainmhithe, ó phlandaí, ó mhiocrorgánaigh, ó fhungais nó algaí, nó atá ar leithlis ó shaothrán cille nó saothrán fiacháin a dhíorthaítear ó ainmhithe, ó phlandaí, ó mhiocrorgánaigh, ó fhungais nó algaí, nó ar táirgeadh é ó shaothrán cille nó saothrán fíocháin a dhíorthaítear ó ainmhithe, ó phlandaí, ó mhiocrorgánaigh, ó fhungais nó algaí...' Tagairt "Rialachán (AE) 2015/2283 maidir le bianna núíosacha, lena leasaítear Rialachán (AE) Uimh. 1169/2011 ó Pharlaimint na hEorpa agus ón gComhairle agus lena n-aisghairtear Rialachán (CE) Uimh. 258/97 ó Pharlaimint na hEorpa agus ón gComhairle agus Rialachán (CE) Uimh. 1852/2001 ón gCoimisiún, CELEX:32015R2283/GA"
    saothrúchán fíocháin Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    saothrán fíocháin plandaí Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Gewebekultur | pflanzliche Gewebekultur | pflanzliche Zellkultur
    de
    Sainmhíniú Methode zur Klonierung von pflanzlichen Zellen bzw. zur vegetativen Vermehrung (in vitro) von Pflanzen unter sterilen Bedingungen Tagairt "Council-DE in Anl. an BM (DE) für Bildung und Forschung, Pflanzenforschung-DE > Gewebekultur (7.11.2023)"
    plant tissue culture | PTC | tissue culture | TC | in vitro culture
    en
    Sainmhíniú cultivation of plant cells, tissues, or organs on specially formulated nutrient media Tagairt "International Service for the Acquisition of Agri-biotech Applications (ISAAA). 'Pocket K No. 14: Tissue Culture Technology' (5.7.2023)"
    Nóta "It is the first step of in vitro propagation"
  14. SOCIAL QUESTIONS|health|medical science
    tástáil trasfhoirmithe ceall Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Zelltransformationstest
    de
    cell-transformation assay | cell transformation test | in vivo tests | in vitro mammalian cell transformation test
    en
    Sainmhíniú test with mammalian cell culture systems used to detect phenotypic changes in vitro induced by chemical substances associated with malignant transformation in vivo Tagairt "COM-EN, based on: Commission Regulation (EC) No 440/2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) CELEX:32008R0440/EN"
    essai de transformation de cellules | test de transformation sur cellules
    fr
  15. AGRICULTURE, FORESTRY AND FISHERIES|agricultural activity|crop production|plant propagation
    micriomadú Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Mikrovermehrung
    de
    Sainmhíniú Multiplikation von Pflanzenmaterial zur Erzeugung einer Vielzahl von Pflanzen mit Hilfe einer In-vitro-Kultur aus ausdifferenzierten vegetativen Knospen bzw. ausdifferenzierten vegetativen Meristemen einer Pflanze Tagairt "Durchführungsrichtlinie 2014/98/EU der Kommission vom 15. Oktober 2014 zur Durchführung der Richtlinie 2008/90/EG des Rates hinsichtlich der spezifischen Anforderungen an die in deren Anhang I aufgeführten Gattungen und Arten von Obstpflanzen, der spezifischen Anforderungen an die Versorger und ausführlicher Bestimmungen für die amtliche Prüfung"
    micropropagation | in vitro vegetative propagation | micro-propagation
    en
    Sainmhíniú "growing of plants from meristematic tissue or somatic cells of superior plants on nutrient suitable media under controlled aseptic physical conditions" Tagairt "theagricos.com > Plant Tissue culture > Micropropagation (5.7.2023)"