This document is an excerpt from the EUR-Lex website
Document 31981L0464
National transposition measures communicated by the Member States concerning:
Council Directive 81/464/EEC of 24 June 1981 amending Council Directive 78/25/EEC on the approximation of the rules of the Member States relating to the colouring matters which may be added to medicinal products
OJ L 183, 04/07/1981, p. 33–33
(DA, DE, EL, EN, FR, IT, NL) This document has been published in a special edition(s)
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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.
Vyhláška č. 228/2008 Sb., o registraci léčivých přípravků
Bekendtgørelse nr. 495 af 12/09/1977
Bekendtgørelse nr. 496 af 12/09/1977
Ravimpreparaatide registreerimiseks vajaliku täiendava dokumentatsiooni eeskiri
Décision ministérielle numéro 9392/91 du 10/03/1992. FEK numéro 233 du 07/04/1992 Page 2258
Οι περί Κτηνιατρικών Φαρμακευτικών Προϊόντων (Χρωστικές Ουσίες) Κανονισμοί του 2001
Οι περί Κτηνιατρικών Φαρμακευτικών Προϊόντων (Χρωστικές Ουσίες) Κανονισμοί του 2006.
1998. évi XXV. törvény az emberi felhasználásra kerülő gyógyszerekről
Ministeriële verordening nummer 133652 van 02/12/1977, Staatscourant nummer 242 van 12/12/1977
Ustawa z dnia 6 września 2001 r. Prawo farmaceutyczne (tekst jednolity)
Lääkelaki (395/87) 10/04/1987, muutos (1046/93) 26/11/1993
Läkemedelslag, Svensk författningssamling SFS) 1992:859
Läkemedelsförordning, Svensk författningssamling SFS) 1992:1752
Leaflet MAL 60, Department of Health and Social Security of June 1979
Regulations 1977. Statutory Instruments number 170 of 1979