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Document 31975L0318
National transposition measures communicated by the Member States concerning:
Rådets direktiv 75/318/EEG av den 20 maj 1975 om tillnärmning av medlemsstaternas lagstiftning om analytiska, farmakologiska, toxikologiska och kliniska normer och prövningsplaner för undersökning av farmaceutiska specialiteter
OJ L 147, 09/06/1975, p. 1–12
(DA, DE, EN, FR, IT, NL) This document has been published in a special edition(s)
(EL, ES, PT, 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. 727 af 09/09/1993
Bekendtgørelse nr. 164 af 13/03/1995
Décision ministérielle numéro A6 9392/91 du 10/03/1992. FEK numéro 233 du 07/04/1992 Page 2258
Koninklijk Besluit van 08/09/1977, Staatsblad nummer 537 van 11/10/1977
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) Regulations 1977. Statutory Instruments number 996 of 1977
The Medicines (Medicines Act 1968) Regulations 1977. Statutory Instruments number 1050 of 1977
The Medicines (Leaflets) Regulations 1977. Statutory Instruments number 1055 of 1977