Vous avez cherché: authorisation (Espagnol - Anglais)

post-authorisation
post-authorisation post-authorisation

definitive authorisation
acreditación definitiva

administrationpost-authorisation
post-authorisation post-authorisation evaluation of evaluation of

marketing authorisation holder
holder

evaluaciÓn deevaluaciÓn de pre-authorisation
pre--authorisation preauthorisation evaluation of evaluation of

at upon receiving authorisation from the buyer for
at upon receiving authorisation from the buyer for

fecha de la primera authorisation: 10 mayo 2010
date of first authorisation: 10 may 2010

plan de autorizaciones previas (advance authorisation scheme);
advance authorisation scheme;

nuevo principio activo, conditionial authorisation, estudios adicionales
new active substance, conditionial authorisation, pass

stability testing for variation to a marketing authorisation type ii marzo de 1997
stability testing for variation to a marketing authorisation type ii

sistema de autorización previa (advance authorisation scheme, «aas»)
advance authorisation scheme (aas)

advance authorisation scheme («aas») (sistema de autorización previa);
advance authorisation scheme (‘aas’);

sistema de autorizaciones previas («advance authorisation scheme», «aas»)
advance authorisation scheme ('aas')

autorización de importación libre de derechos (duty free import authorisation, «dfia»);
duty free import authorisation (dfia);

standard operating procedure on the release of assessment reports to applicants / marketing authorisation holders
standard operating procedure on the release of assessment reports to applicants/ marketing authorisation holders

13the european agency for the evaluation of medicinal products pre-authorisation evaluation of medicines for human use
cpmp/4082/0016/16the european agency for the evaluation of medicinal products pre-authorisation evaluation of medicines for human use

pre-authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products
pre-authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products

carcinogenicity testing pre-authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products
carcinogenicity testing pre-authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products

cpmp/ qwp/ 576/ 96 note for guidance on stability testing for a type ii variation to a marketing authorisation
note for guidance on stability testing for a type ii variation to a marketing authorisation

position paper on the regulatory requirements for the authorisation of low-dose modified release asa formulations in the secondary prevention of cardiovascular events.
position paper on the regulatory requirements for the authorisation of low-dose modified release asa formulations in the secondary prevention of cardiovascular events.