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Document 31981L0464
National transposition measures communicated by the Member States concerning:
Id-Direttiva tal-Kunsill ta’ l-24 ta’ Ġunju 1981 li temenda d-Direttiva tal-Kunsill 78/25/KEE dwar l-approssimazzjoni tar-regoli ta’ l-Istati Membri li ghandhom x’jaqsmu mal-materji kuluranti li jistgħu jiġu miżjuda mal-prodotti mediċinali
OJ L 183, 04/07/1981, p. 33–33
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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