This document is an excerpt from the EUR-Lex website
Document 31975L0318
National transposition measures communicated by the Member States concerning:
Direttiva 75/318/CEE del Consiglio, del 20 maggio 1975, relativa al ravvicinamento delle legislazioni degli Stati Membri riguardanti le norme ed i protocolli analitici, tossicofarmacologici e clinici in materia di sperimentazione delle specialità medicinali
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