Je was op zoek naar: authorisation (Portugees - Duits)

post- authorisation
beurteilung von

marketing authorisation suspended
authorisation suspended

pre- authorisation avaliaÇÃo de
post-authorisation

notice to marketing authorisation holders – pharmacovigilance guidlines
notice to marketing authorisation holders – pharmacovigilance guidlines

european medicines agency post- authorisation evaluation of medicines for human use
european medicines agency post-authorisation evaluation of medicines for human use

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

{name of the marketing authorisation holder} [a ser completado nacionalmente]
{inhaber der zulassung} [ist national auszufüllen]

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

the european agency for the evaluation of medicinal products pre- authorisation evaluation of medicines for human use
the european agency for the evaluation of medicinal products beurteilung von humanarzneimitteln vor der zulassung

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

use of near infra- red spectroscopy by the pharmaceutical industry and the data to be forwarded in part ii of the dossier for a marketing authorisation
use of near infra-red spectroscopy by the pharmaceutical industry and the data to be forwarded in part ii of the dossier for 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.

análise da introdução de um sistema electrónico de autorização de viagem (electronic system of travel authorisation – esta).
die prüfung der einführung eines systems zur elektronischen erteilung von reisebewilligungen (electronic system of travel authorisation – esta).

contribution to part s. 2. 3 of the structure of the dossier for applications for marketing authorisation – control of starting materials for the production of plasma- derived medicinal products
contribution to part s.2.3 of the structure of the dossier for applications for marketing authorisation – control of starting materials for the production of plasma-derived medicinal products

o sistema proposto é designado reach, que é o acrónimo de registo, avaliação e autorização de substâncias químicas (registration, evaluation and authorisation of chemicals).
das vorgeschlagene system wird reach genannt, ein akronym für registration (registrierung), evaluation (bewertung) und authorisation (zulassung) von chemicals (chemikalien).

4.5 um estudo de segurança após autorização (post-authorisation safety study - pass) é um estudo científico que tem por objetivo avaliar a segurança dos medicamentos.
4.5 eine sicherheitsstudie nach der zulassung (post-authorisation safety study - pass) ist eine wissenschaftliche studie, die der arzneimittelsicherheit dient.