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Document 32009L0035
National transposition measures communicated by the Member States concerning:
Οδηγία 2009/35/ΕΚ του Ευρωπαϊκού Κοινοβουλίου και του Συμβουλίου, της 23ης Απριλίου 2009 , σχετικά με τις ουσίες που μπορούν να προστεθούν στα φάρμακα για τον χρωματισμό (αναδιατύπωση) (Κείμενο που παρουσιάζει ενδιαφέρον για τον ΕΟΧ)
OJ L 109, 30/04/2009, p. 10–13
(BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV) This document has been published in a special edition(s)
(HR)
The member states bear sole responsibility for all information on this site provided by them on the transposition of EU law into national law. This does not, however, prejudice the results of the verification by the Commission of the completeness and correctness of the transposition of EU law into national law as formally notified to it by the member states. The collection National transposition measures is updated weekly.
Vyhláška č. 228/2008 Sb., o registraci léčivých přípravků
Vyhláška č. 13/2010 Sb., kterou se mění vyhláška č. 228/2008 Sb., o registraci léčivých přípravků
Vyhláška č. 235/2010 Sb., o stanovení požadavků na čistotu a identifikaci přídatných látek
EM estime MNE non nécessaire - MS does not consider NEM necessary.
EM estime MNE non nécessaire - MS does not consider NEM necessary.
Pravilnik o davanju odobrenja za stavljanje lijeka u promet
EM estime MNE non nécessaire - MS does not consider NEM necessary.