Results for authorisation translation from Dutch to German

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Dutch

pre-authorisation

German

pre- authorisation

Last Update: 2012-04-11
Usage Frequency: 2
Quality:

Dutch

marketing authorisation suspended

German

matrixgekoppelte, kultivierte und charakterisierte, autologe chondrozyten

Last Update: 2017-04-26
Usage Frequency: 1
Quality:

Dutch

beoordeling ge- post-authorisation

German

post-authorisation

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

marketing authorisation number(s)

German

zulassungsnummer(n)

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

name of the marketing authorisation holder

German

name des pharmazeutischen unternehmers

Last Update: 2012-04-11
Usage Frequency: 2
Quality:

Dutch

(post-authorisation efficacy study, paes):

German

einschließlich beatmungsassoziierter pneumonien, bei hospitalisierten

Last Update: 2017-04-26
Usage Frequency: 1
Quality:

Dutch

name and address of the marketing authorisation holder

German

name und anschrift des pharmazeutischen unternehmers

Last Update: 2012-04-11
Usage Frequency: 2
Quality:

Dutch

notice to marketing authorisation holders – pharmacovigilance guidlines

German

notice to marketing authorisation holders – pharmacovigilance guidlines

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

non-interventional post-authorisation safety study (pass):

German

nichtinterventionelle unbedenklichkeitsprüfung nach der zulassung (pass): studie ac-052-516:

Last Update: 2017-04-26
Usage Frequency: 1
Quality:

Dutch

advance authorisation scheme (regeling voorafgaande vergunningen, „aas”)

German

advance authorisation scheme („aas“) — vorabgenehmigungsregelung

Last Update: 2014-11-12
Usage Frequency: 1
Quality:

Dutch

non-interventional post-authorisation safety study (pass) om de

German

nichtinterventionelle unbedenklichkeitsprüfung nach der zulassung (pass)

Last Update: 2017-04-26
Usage Frequency: 1
Quality:

Dutch

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

German

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

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

note for guidance on stability testing for a type ii variation to a marketing authorisation

German

note for guidance on stability testing for a type ii variation to a marketing authorisation

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

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

German

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

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

the european agency for the evaluation of medicinal products pre-authorisation evaluation of medicines for human use

German

the european agency for the evaluation of medicinal products pre-authorisation evaluation of medicines for human use

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

marketing authorisation holder merck sharp & dohme limited hertford road, hoddesdon hertfordshire en11 9bu verenigd koninkrijk

German

hertford road, hoddesdon hertfordshire en11 9bu vereinigtes königreich

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

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

German

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

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

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

German

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

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

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

German

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

Last Update: 2011-10-23
Usage Frequency: 1
Quality:

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Dutch

na jaren voorbereiding is reach — registration, evaluation, authorisation and restriction of chemicals29— in juni in werking getreden.

German

nach jahrelanger vorbereitung wurde die reach-verordnung – über die registrierung, bewertung, zulassung und beschränkung chemischer stoffe29 – im juni endlich operativ.

Last Update: 2017-04-07
Usage Frequency: 1
Quality:

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