This document is an excerpt from the EUR-Lex website
Document 31987L0019
National transposition measures communicated by the Member States concerning:
Directiva 87/19/CEE del Consejo de 22 de diciembre de 1986 por la que se modifica la Directiva 75/318/CEE relativa a la aproximación de las legislaciones de los Estados Miembros sobre normas y protocolos analíticos, tóxico-farmacológicos y clínicos en materia de pruebas de especialidades farmacéuticas
OJ L 15, , pp. 31–33
(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.
Bekendtgørelse nr. 451 af 06/08/1982
Décision ministérielle numéro 3588-3783/16728 du 21/09/1987. FEK numéro 351 du 06/07/1987
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 41.448/57 de 18/12/1957
Lääkelaki (395/87) 10/04/1987, muutos (1046/93) 26/11/1993
Läkemedelslag, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752