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Document 31987L0021
National transposition measures communicated by the Member States concerning:
Οδηγία 87/21/ΕΟΚ του Συμβουλίου της 22ας Δεκεμβρίου 1986 για την τροποποίηση της οδηγίας 65/65/ΕΟΚ περί της προσέγγισης των νομοθετικών, κανονιστικών και διοικητικών διατάξεων σχετικά με τα φαρμακευτικά ιδιοσκευάσματα
OJ L 15, 17/01/1987, p. 36–37
(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. 451 af 06/08/1982
Besluit van 17/04/1986 regeling registratie diergeneesmiddelen, Staatscourant nummer j.7027 van 1986
Besluit van 19/11/1987 j.7763, Staatscourant nummer 229 van 1987
Decreto-lei numero 41448/57 de 18/12/1957. Diário da Republica I Série de 18/12/1957
Lääkelaki (395/87) 10/04/1987, muutos (1046/93) 26/11/1993
Lääkeasetus (693/87) 24/07/1987, muutos (1490/93) 22/12/1993
Hallintomenettelylaki (598/82) 06/08/1982
Tuotevastuulaki (694/90) 17/10/1990, muutos (99/93) 08/01/1993
Läkemedelslag, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752
Förvaltningslag, Svensk författningssamling SFS) 1986:223
Produktansvarslag, Svensk författningssamling SFS) 1992:18