This document is an excerpt from the EUR-Lex website
Document 31989L0342
National transposition measures communicated by the Member States concerning:
Council Directive 89/342/EEC of 3 May 1989 extending the scope of Directives 65/65/EEC and 75/319/EEC and laying down additional provisions for immunological medicinal products consisting of vaccines, toxins or serums and allergens
OJ L 142, 25/05/1989, p. 14–15
(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.
Lov 40 nr. 8 hvorefter visse vacciner kan forhandles uden godkendelse
Bekendtgørelse nr. 777 af 12/12/1989
Décision ministérielle numéro A6A/9392/91 du 10/03/1992. FEK numéro 233 du 07/04/1992 Page 2257
Lääkelaki (395/87) 10/04/1987, muutos (1046/93) 26/11/1993
Läkemedelslagen, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752
The Medicines Act 1968 (Amendment) Regulations 1992. Statutory Instruments number 604 of 1992