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 »

1 toradh

  1. ENVIRONMENT|deterioration of the environment|nuisance · SOCIAL QUESTIONS|health|health policy|organisation of health care|public health|health risk
    measúnú riosca don chomhshaol Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Comhthéacs 'Déanfar measúnú ar shábháilteacht úsáideoirí, measúnú riosca don chomhshaol, staidéir ar ídiú iarmhar, agus staidéir chliniciúla maidir leis an táirge comhcheangailte seasta.' Tagairt "Rialachán Tarmligthe (AE) 2021/805 ón gCoimisiún an 8 Márta 2021 lena leasaítear Iarscríbhinn II a ghabhann le Rialachán (AE) 2019/6 ó Pharlaimint na hEorpa agus ón gComhairle, CELEX:32021R0805/GA"
    measúnú riosca comhshaoil Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    measúnú ar an mbaol don chomhshaol Tagairt an Ghníomhaireacht Eorpach Comhshaoil (GEC)
    ga
    Umweltverträglichkeitsprüfung
    de
    environmental risk assessment | ERA
    en
    Sainmhíniú evaluation of risks posed to human health and the environment - whether direct or indirect, immediate or delayed, due to the production/manufacturing of a substance, its use and its disposal - included in marketing authorisation applications for medicinal products in the European Union Tagairt "COM-Terminology Coordination, based on:1) Directive 2001/18/EC on the deliberate release into the environment of genetically modified organisms and repealing Directive 90/220/EEC2) European Commisison. Health & Consumer Protection Directorate-General. 'Report on the ecological risk assessment of chemicals' (27.11.2023) discussed by the scientific steering committee at its meeting of 7-8 November 20023) Proposal for a Directive on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC, COM(2023) 192"
    Nóta For medicinal product with an antimicrobial mode of action, the ERA also encompasses an evaluation of the risk for antimicrobial resistance selection in the environment due to the manufacturing, use and disposal of that medicinal product.
    évaluation des risques pour l’environnement
    fr
    Sainmhíniú évaluation des risques, directs ou indirects, immédiats ou différés, que la dissémination volontaire ou la mise sur le marché d'OGM peut comporter pour la santé humaine et l'environnement Tagairt "COM-FR d'après Directive 2001/18/CE du Parlement européen et du Conseil du 12 mars 2001 relative à la dissémination volontaire d'organismes génétiquement modifiés dans l'environnement et abrogeant la directive 90/220/CEE du Conseil"