Examples of using Labelling and package leaflet in English and their translations into Dutch
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Computer
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Ecclesiastic
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Official/political
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Programming
Labelling and package leaflet.
For harmonised labelling and package leaflet.
Labelling and package leaflet.
Characteristics, labelling and package leaflet.
Labelling and package leaflet.
Summary of product characteristics, labelling and package leaflet.
Labelling and package leaflet.
Summary of product characteristics, labelling and package leaflet.
Labelling and package leaflet.
Summary of product charachteritics, labelling and package leaflet.
Labelling and package leaflet.
Rational use of medicinal products: labelling and package leaflet 5.21.
Labelling and package leaflet.
Summary of product characteristics, labelling and package leaflet.
Labelling and package leaflet isa or uth ga tin ker ma.
The legibility of particulars on the labelling and package leaflet.
Annex iii labelling and package leaflet.
Grounds for amendment of the summary of product characteristics, labelling and package leaflet.
SmPC, labelling and package leaflet should reflect the presence of a score.
The Summaries of Products Characteristic, labelling and package leaflet proposed by the Marketing.
The scope of the referral was the harmonisation of the Summary of Product Characteristics, labelling and package leaflet.
The most recent labelling and package leaflet as approved by the competent authorities;
The scientific conclusions are provided in Annex II together with the amended SPC, Labelling and Package Leaflet in Annex III.
General conditions: labelling and package leaflet of medicinal products for human consumption.
The Summaries of Products Characteristic, labelling and package leaflet proposed by the Marketing.
Proposal for a Council directive on the labelling and package leaflet of medicinal products for human consumption.
The Summary of Product Characteristics, Labelling and Package Leaflet of the Reference Member State should be amended.
Council Directive 92/27/EEC of 31 March 1992 on the labelling and package leaflet of medicinal products for human consumption.
It must not contradict the summary of product characteristics, labelling and package leaflet of the medicinal product, as approved by the competent authorities.