This document is an excerpt from the EUR-Lex website
Document 31983L0570
National transposition measures communicated by the Member States concerning:
Council Directive 83/570/EEC of 26 October 1983 amending Directives 65/65/EEC, 75/318/EEC and 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products
OJ L 332, 28/11/1983, p. 1–10
(DA, DE, EL, EN, FR, IT, NL) This document has been published in a special edition(s)
(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.
Sundhedsstyrelsen Meddelelse af den 22/08/1985
Sundhedsstyrelsen Meddelelse af den 12/05/1986
Décision ministérielle numéro A6/10395. FEK numéro 798 du 31/12/1985
Avis (notes explicatives concernant essais mise sur marché), Journal Officiel du 05/12/1985
Arrêté ministériel du 02/10/1985 (essais toxico-pharmacologiques), Journal Officiel du 15/10/1986
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
The Guidance Notes on Applications for Product Licences MAL (No. 2) of 31/07/1985
The Medicines (Labelling) (Amendment) Regulations 1985. Statutory Instruments number 1558 of 1985