Examples of using Labelling and package leaflet in English and their translations into Polish
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Financial
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Official/political
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Programming
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Computer
for which the Summary of Product Characteristics, labelling and package leaflet are set out in Annex III for Lamictal and associated names see Annex I.
Organon presented to the EMEA a referral under Article 30 of Directive 2001/ 83/ EC, as amended, in order to harmonise the nationally authorised Summaries of Product Characteristics(SPC), Labelling and Package Leaflet, including quality aspects of the medicinal product Remeron and associated names.
for which the Summary of Product Characteristics, labelling and package leaflet are set out in Annex III for Lisonorm and associated names see Annex I.
was of the opinion that the proposal for the harmonisation of the SPC, Labelling and Package Leaflet was acceptable
The CHMP has recommended the granting of the Marketing Authorisations for which the Summary of Product Characteristics, labelling and package leaflet remain as per the final versions achieved during the Coordination Group procedure as mentioned in Annex III for UMAN BIG.
was of the opinion that the proposal for the harmonisation of the SPC, Labelling and Package leaflet was acceptable
was of the opinion that the proposal for the harmonisation of the SPC, Labelling and Package Leaflet was acceptable
was of the opinion that the proposal for the harmonisation of the SPC, Labelling and Package leaflet was acceptable
as amended, in order to harmonise the nationally authorised Summaries of Product Characteristics(SPC), Labelling and Package Leaflet including quality aspects of the medicinal product Singulair and associated names.
On 9 October 2007 the Commission presented to the EMEA a referral under Article 30 of Directive 2001/ 83/ EC, as amended, in order to harmonise the nationally authorised Summaries of Product Characteristics(SPC), Labelling and Package Leaflet of the medicinal product Zyrtec and associated names.
This Annex III(Summary of Product Characteristics, Labelling and Package Leaflet) is the one that was Annexed to the Commission Decision on this Article 6(13)
together with the amended Summary of Product Characteristics, Labelling and Package Leaflet in the Annex III
for which the Summaries of Product Characteristics, labelling and package leaflet are set out in Annex III for Nifedipinr Pharmamatch Retard 30/ 60 mg
On 3 May 2007, the European Commission presented to the EMEA a referral under Article 30 of Directive 2001/ 83/ EC, as amended, in order to harmonise the nationally authorised Summaries of Product Characteristics(SPC), Labelling and Package Leaflet of the medicinal product Efexor depot.
was of the opinion that the proposal for the harmonisation of the SPC, Labelling and Package leaflet including the quality aspects was acceptable
Specific rules should be laid down, adapting the requirements in Directive 2001/83/EC as regards the summary of product characteristics, labelling and package leaflet to the technical specificities of advanced therapy medicinal products.
the scientific discussion within the Committee, was of the opinion that the proposal for the harmonisation of the SPC, Labelling and Package leaflet including the quality aspects was acceptable and that they should be amended.
The EESC is pleased that the summary of product characteristics, labelling and package leaflet of the medicinal product,
The proposal for a Directive is rightly based on the principle that officially approved information such as the summary of product characteristics, labelling and package leaflet of the medicinal product,
a Marketing Authorisation and that the Summary of Product Characteristics, labelling and package leaflet of the Reference Member State should be amended.