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- biokema - eea
- biokema - eea
Laatste Update: 2011-10-23
Gebruiksfrequentie: 1
Kwaliteit:
Gelieve het te verwijderen indien je dit meent.
[34] eea 2005.
[34] ema 2005.
Laatste Update: 2008-03-04
Gebruiksfrequentie: 2
Kwaliteit:
Referentie:
[33] soe, eea, 2005.
[33] soe (toestand van het milieu), ema, 2005.
Laatste Update: 2008-03-04
Gebruiksfrequentie: 2
Kwaliteit:
Referentie:
[4] Αναλήψεις υποχρεώσεων eea 52051 και eea 52049.
[4] vastleggingen eea 52051 en eea 52049.
Laatste Update: 2008-03-04
Gebruiksfrequentie: 2
Kwaliteit:
Referentie:
Η άδεια κυκλοφορίας αυτού του φαρµακευτικού προϊόντος έχει εγκριθεί στις χώρες µέλη της eea υπό τις εξής ονοµασίες:
dit geneesmiddel is geregistreerd in lidstaten van de eea onder de volgende namen:
Laatste Update: 2012-04-12
Gebruiksfrequentie: 2
Kwaliteit:
Referentie:
1 Κράτος Μέλος Κάτοχος Αδείας Κυκλοφορίας, Αιτούντας (Επινοηθείσα) Ονομασία eu/ eea
1 lidstaat eu/eea
Laatste Update: 2011-10-23
Gebruiksfrequentie: 1
Kwaliteit:
Referentie:
Gelieve het te verwijderen indien je dit meent.
(37) the commission warns the united kingdom of great britain and northern ireland that it will inform interested parties by publishing this letter and a meaningful summary of it in the official journal of the european union. it will also inform interested parties in the efta countries which are signatories to the eea agreement, by publication of a notice in the eea supplement to the official journal of the european union and will inform the efta surveillance authority by sending a copy of this letter. all such interested parties will be invited to submit their comments within one month of the date of such publication."
(37) the commission warns the united kingdom of great britain and northern ireland that it will inform interested parties by publishing this letter and a meaningful summary of it in the official journal of the european union. it will also inform interested parties in the efta countries which are signatories to the eea agreement, by publication of a notice in the eea supplement to the official journal of the european union and will inform the efta surveillance authority by sending a copy of this letter. all such interested parties will be invited to submit their comments within one month of the date of such publication.%quot%
Laatste Update: 2008-03-04
Gebruiksfrequentie: 6
Kwaliteit:
Referentie:
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