This document is an excerpt from the EUR-Lex website
Document 32009L0035
National transposition measures communicated by the Member States concerning:
Europa-Parlamentets og Rådets direktiv 2009/35/EF af 23. april 2009 om stoffer, der må tilsættes lægemidler med henblik på farvning af disse (omarbejdning) (EØS-relevant tekst)
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.