This document is an excerpt from the EUR-Lex website
Document 31987L0022
National transposition measures communicated by the Member States concerning:
Council Directive 87/22/EEC of 22 December 1986 on the approximation of national measures relating to the placing on the market of high-technology medicinal products, particularly those derived from biotechnology
OJ L 15, 17/01/1987, p. 38–41
(ES, DA, DE, EL, EN, FR, IT, NL, PT)
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
Verordnung vom 24/11/1993, Bundesgesetzblatt Teil I
Bekanntmachung vom 30/06/1987, Bundesanzeiger Nr. 118 vom 02/07/1987
Décision ministérielle numéro 3588-3783/16914 du 24/09/1987. FEK numéro 388 du 27/07/1987
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 n. 41448/57 de 18/12/1957. Diário da República I Série de 18/12/1957
Läkemedelslag, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752