Vous avez cherché: comparability (Danois - Allemand)

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comparability

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Danois

Allemand

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Danois

lack of comparability of skills/ qualifications;

Allemand

mängel in der vergleichbarkeit von kompetenzen/ berufsabschlüssen;

Dernière mise à jour : 2017-04-07
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Danois

note for guidance on comparability of medicinal products containing biotechnology- derived proteins as active substances

Allemand

declaration of storage conditions for veterinary medicinal products in the product particulars verabschiedet im februar 2000

Dernière mise à jour : 2011-10-23
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Danois

such comparability is requested by all users , not only at community level , but also within member states .

Allemand

such comparability is requested by all users , not only at community level , but also within member states .

Dernière mise à jour : 2011-10-23
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Danois

konceptdokumenter concept paper om gene therapy concept paper on the development of a cpmp guideline on comparability of biotechnology- derived products

Allemand

concept paper on gene therapy concept paper on the development of a cpmp guideline on comparability of b iotechnology-derived products

Dernière mise à jour : 2011-10-23
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Danois

community legislation on statistics on the structure and activity of foreign affiliates is needed to set common statistical standards for data , with a high degree of comparability between data colleted in different member states .

Allemand

community legislation on statistics on the structure and activity of foreign affiliates is needed to set common statistical standards for data , with a high degree of comparability between data colleted in different member states .

Dernière mise à jour : 2011-10-23
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Danois

from 5 december 2005 release, eurostat implements a refined definition of the educational attainment level "upper secondary" in order to increase the comparability of results in the eu.

Allemand

from 5 december 2005 release, eurostat implements a refined definition of the educational attainment level "upper secondary" in order to increase the comparability of results in the eu.

Dernière mise à jour : 2014-10-23
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Danois

63) note for guidance on photosafety testing points to consider document on the need for assessment of reproductive toxicity of human insulin analogues discussion paper on environmental risk assessments of non- gmo containing medicinal products for human use non- clinical documentation of medicinal products with ‘ well- established use ’ note for guidance on the need for non- clinical testing of pharmaceuticals in juvenile animals discussion paper on the non- clinical safety studies to support single low dose clinical screening studies in man note for guidance on specification limits for residues for heavy metal catalysts in medicinal products points to consider on xenogeneic cell therapy note for guidance on comparability of biotechnology products pre- clinical and clinical issues points to consider on the assessment of the potential for qt interval prolongation by non- cardiovascular medicinal products note for guidance on risk assessment of medicinal products on human reproductive and development toxicities: from data to labelling

Allemand

63) note for guidance on photosafety testing points to consider document on the need for assessment of reproductive toxicity of human insulin analogues discussion paper on environmental risk assessments of non-gmo containing medicinal products for human use non-clinical documentation of medicinal products with ‘ well-established use’ note for guidance on the need for non-clinical testing of pharmaceuticals in juvenile animals discussion paper on the non-clinical safety studies to support single low dose clinical screening studies in man note for guidance on specification limits for residues for heavy metal catalysts in medicinal products points to consider on xenogeneic cell therapy note for guidance on comparability of biotechnology products pre-clinical and clinical issues points to consider on the assessment of the potential for qt interval prolongation by non-cardiovascular medicinal products note for guidance on risk assessment of medicinal products on human reproductive and development toxicities: from data to labelling

Dernière mise à jour : 2011-10-23
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