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Document 31992L0027
National transposition measures communicated by the Member States concerning:
Richtlijn 92/27/EEG van de Raad van 31 maart 1992 betreffende de etikettering en de bijsluiter van geneesmiddelen voor menselijk gebruik
OJ L 113, 30/04/1992, p. 8–12
(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.
Bekendtgørelse nr. 314 af 18/05/1993
Bekendtgørelse nr. 642 af 02/08/1993 om recepter
Décision ministérielle numéro Y6A/776/1993 du 23/06/1993. FEK numéro 536 du 20/07/1993 Page 5847
Correction des erratas Décision ministérielle. FEK numéro 745 du 27/09/1993 Page 7841
Lääkelaki (395/87) 10/04/1987, muutos (1046/93) 26/11/1993
Läkemedelslag, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752
The Medicines (Labelling) Amendment Regulations 1992. Statutory Instruments number 3273 of 1992
The Medicines (Leaflets) Amendment Regulations 1992. Statutory Instruments number 3274 of 1992