This document is an excerpt from the EUR-Lex website
Document 31992L0018
National transposition measures communicated by the Member States concerning:
Direttiva 92/18/CEE della Commissione, del 20 marzo 1992, che modifica l'allegato della direttiva 81/852/CEE del Consiglio per il ravvicinamento delle legislazioni degli Stati Membri relative alle norme e ai protocolli analitici, tossico- farmacologici e clinici in materia di prove effettuate su medicinali veterinari
OJ L 97, 10/04/1992, p. 1–23
(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.
Arrêté royal du 22/09/92. Moniteur belge
Bekendtgørelse nr. 452 af 10/06/1992
Bekendtgørelse nr. 727 af 09/09/1993
Arzneimittelgesetz vom 19/10/1994, Bundesgesetzblatt Teil I vom 27/10/1994 Seite 3018
Arrêté ministériel numéro 399886 du 09/09/1994. FEK numéro 741 du 04/10/1994 Page 6917
Décision ministérielle numéro 310584 du 02/04/1998. FEK numéro 456 du 15/05/1998 Page 4807
Wijziging Regeling registratie diergeneesmiddelen, Staatscourant nummer 62 van 30/03/1993
Regeling registratie diergeneesmiddelen van 1992, Staatscourant nummer 185
Gewerbeordnung BGBl. Nr. 194/1994
Lääkelaki (395/87) 10/04/1987, muutos (1046/93) 26/11/1993
Läkemedelslag, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752