TMS.3.0.2007

R.10 Transfusionsmedicinske Standarder. Version 3.0
R.500 Europarådet
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.
Transport and international exchange of substances of human
origin. Recommendation No. (79) 5.
Blood products for the treatment of haemophiliacs.
Recommendation No. R (80) 5.
Antenatal administration of anti-D immunoglobulin.
Recommendation No. R (81) 5.
Assessment of the risks of transmitting infectious diseases by
international transfer of blood, its components and derivatives.
Recommendation No. R (81) 14.
Preventing the possible transmission of acquired immune
deficiency syndrome (AIDS) from affected blood to patients
receiving blood or blood products. Recommendation No. R (83) 8.
Prevention of the transmission of malaria by blood transfusion.
Recommendation No. R (84) 6.
© 1994-2007 Dansk Selskab for Klinisk Immunologi