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. EUROPEAN UNION|EU institutions and European civil service|EU office or agency|European Medicines Agency
    ceadú rialála mear Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    faomhadh rialála mear Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    formheas rialála mear Tagairt Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    fast track regulatory approval | fast regulatory approval | fast-tracking regulatory approval
    en
    Sainmhíniú accelerated assessment and conditional marketing authorisation for innovative medicines that target a disease for which no treatment is available, or that provide patients with a major therapeutic advantage over existing treatments Tagairt "EMA. 'Fast track routes for medicines that address unmet medical needs' (22.2.2021). News 27/07/2015"