This document is an excerpt from the EUR-Lex website
Document 32011L0038
National transposition measures communicated by the Member States concerning:
Uitvoeringsrichtlijn 2011/38/EU van de Commissie van 11 april 2011 tot wijziging van bijlage V bij Richtlijn 2004/33/EG ten aanzien van maximale pH-waarden voor trombocytenconcentraten tegen het einde van de bewaartermijn Voor de EER relevante tekst
OJ L 97, 12/04/2011, p. 28–29
(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.
Zákon č. 378/2007 Sb., o léčivech a o změnách některých souvisejících zákonů (zákon o léčivech)
Bekendtgørelse om ændring af bekendtgørelse om kvalitets- og sikkerhedskrav til blodbankvirksomhed
EM estime MNE non nécessaire - MS does not consider NEM necessary.
Décision du 20 octobre 2010 fixant la liste et les caractéristiques des produits sanguins labiles
Pravilnik o posebnim tehničkim zahtjevima za krv i krvne pripravke
Pravilnik o izmjenama Pravilnika o posebnim tehničkim zahtjevima za krv i krvne pripravke
Pravilnik o izmjeni Pravilnika o posebnim tehničkim zahtjevima za krv i krvne pripravke
Ο Περί Αιμοδοσίας (Τροποποιητικός) Νόμος του 2011.
Verordnung, mit der die Verordnung betreffend Arzneimittel aus menschlichem Blut geändert wird
Ustawa z dnia 22 sierpnia 1997 r. o publicznej służbie krwi.
Blood Safety and Quality Regulations 2005
PUBLIC HEALTH (BLOOD SAFETY AND QUALITY) ACT 2007
Public Health (Blood Safety and Quality) Act 2007 (Amendment) Regulations 2011