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

pre- authorisation
pre- authorisation

marketing authorisation number(s)
markedsfØringstilladelsesnummer (-numre)

advance authorisation scheme („aas“) — vorabgenehmigungsregelung
advance authorisation scheme (aas) (forhåndstilladelsesordningen)

nicht-interventionelle unbedenklichkeitsprüfung (post-authorisation
en ikke-interventionssikkerhedsundersøgelse efter tilladelse til

name and address of the marketing authorisation holder
navn og adresse pÅ indehaveren af markedsfØringstilladelsen

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

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 pre- authorisation evaluation of medicines for human use

es soll eine „post-authorisation safety study“ (pass) anhand einer retrospektiven
et retrospektivt studie med skematisk gennemgang af sikkerheden efter

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.

http://ec.europa.eu/food/plant/gmo/authorisation/index_en.htm
http://ec.europa.eu/food/plant/gmo/authorisation/index_en.htm.

die prüfung der einführung eines systems zur elektronischen erteilung von reisebewilligungen (electronic system of travel authorisation – esta).
undersøgelse af mulighederne for at indføre et elektronisk system for rejsetilladelser (esta).

im interesse der klarheit und einheitlichkeit sollte in der englischen fassung das wort "approval" durch "authorisation" ersetzt werden.
af hensyn til tydelighed og konsekvens ændres ordet "approval" i den engelske tekst til "authorization" (o.a.: på dansk benyttes i dette tilfælde godkendelse for begge ord).

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

4.5 eine sicherheitsstudie nach der zulassung (post-authorisation safety study – pass) ist eine wissenschaftliche studie, die der arzneimittelsicherheit dient.
4.5 en sikkerhedsundersøgelse efter tilladelse til markedsføring (post-authorisation safety study – pass) er en videnskabelig studie med fokus på lægemiddelsikkerhed.

gleichzeitig gewährleistet die neue strategie, dass die industrie ihren weltweiten wettbewerbsvorsprung behält. die vorschläge sind unter dem kürzel reach (registration, evaluation and authorisation of chemicals) bekannt.
den giveroffentligheden vished for, at kemikalier overholder strenge sundheds- og miljønormer, ogsikrer samtidig industriens globale konkurrenceevne. disse udkast til ny politik, der bærer forkortelsen reach (registration, evaluation and authorisation of chemicals) er for tidenunder udarbejdelse i samråd med et bred udvalg af de berørte parter.