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Document 31991L0356
National transposition measures communicated by the Member States concerning:
Commission Directive 91/356/EEC of 13 June 1991 laying down the principles and guidelines of good manufacturing practice for medicinal products for human use
OJ L 193, 17/07/1991, p. 30–33
(ES, DA, DE, EL, EN, FR, IT, NL, PT) This document has been published in a special edition(s)
(FI, SV)
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.
EM estime MNE non nécessaire - MS does not consider NEM necessary.
Bekendtgørelse nr. 796 af 21/09/1992
Décision ministérielle numéro Y.6/11228/93 du 06/04/1993. FEK numéro 322 du 06/05/1993 Page 3599
Οι περί Φαρμάκων Ανθρώπινης Χρήσης (Έλεγχος Ποιότητας, Προμήθειας και Τιμών) Νόμος του 2001
Lääkelaki (395/87) 10/04/1987, muutos (1046/93) 26/11/1993
Lääkeasetus (693/87) 24/07/1987, muutos (1490/93) 22/12/1993
Läkemedelslag, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752