TMS.2.3.2004

R.10 Transfusionsmedicinske Standarder. Version 2.0
R.450 Øvrige initiativer
Protokol til den europæiske overenskomst om udveksling af
terapeutiske stoffer af menneskelig oprindelse. EFT L 37 af
07/02/1987 s. 4.
Europa-parlamentets og Rådets beslutning nr. 2119/98/EF af 24.
September 1998 om oprettelse af et net til epidemiologisk overvågning
af og kontrol med overførbare sygdomme i Fællesskabet. EFT
L 268 af 03/10/1998 s. 1.
R.490 Publikationer
R.500 Europarådet
Commission of the European Communities. The rules governing
medicinal products in the European Community. Volumen I.
November 1993.
Commission of the European Communities. Notice to applicants
for marketing authorization for medicinal products for human use
in the member states of the European Community. Volume IIA
1993. July 1993.
Commission of the European Communities. The rules governing
medicinal products in the European Community. Guidelines on the
quality, safety and efficacy of medicinal products for human use.
Volumen III. January 1989.
Commission of the European Communities. The rules governing
medicinal products in the European Community. Guidelines on the
quality, safety and efficacy of medicinal products for human use.
Addendum. July 1990.
Commission of the European Communities. Good manufacturing
practice for medicinal products in the European Community. The
rules governing medicinal products in the European Community.
Volume IV. January 1992.
R.501 Konventioner og aftaler
European Agreement on the Exchange of Therapeutic Substances of
Human Origin (ETS no. 26, 1958).
European Agreement on the Exchange of Blood Grouping Reagents
(ETS no. 39, 1962).
European Agreement on the Exchange of Tissue-Typing Reagents (ETS
no. 84, 1974).
R.502 Resolutioner og rekommandationer
Harmonisation of legislation of member States relating to removal,
grafting and transplantation of human substanses. Resolution (78)
29.
© 1994-2004 Dansk Selskab for Klinisk Immunologi