TMS.2.3.2004

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viii Transfusionsmedicinske Standarder. Version 2.3 A3.930 Blod til eget brug: blodet anvendes ikke A3.10 APPENDIKS 4 A4.000 GMP regler ved anvendelse af edb-systemer i blodbanker A4.1 A4.100 Personale A4.1 A4.200 Validering A4.1 A4.300 Edb-systemet A4.1 APPENDIKS 5 A5.000 Elektronisk forligelighed A5.1 A5.100 Baggrund A5.1 A5.200 Blodportionen A5.1 A5.300 Patienten A5.1 A5.400 Godkendelse A5.2 A5.500 Validering A5.2 APPENDIKS 6 A6.000 ISBT 128 A6.1 A6.100 Generelt A6.1 A6.200 Datastrukturer A6.3 A6.300 Sammenkædning af stregkoder A6.25 A6.400 Opbygningen af produktkoder A6.25 A6.500 ISBT 128 etikettens udformning A6.28 A6.600 Posefabrikantens etiket A6.34 A6.700 Princip for blodbankens etikettering A6.34 A6.800 Andre anvendelser for ISBT 128 A6.39 APPENDIKS 7 A7.000 Danske blodbanker og deres ISBT 128 identifikationskoder A13.1 © 1994-2004 Dansk Selskab for Klinisk Immunologi
Transfusionsmedicinske Standarder. Version 2.3 ix APPENDIKS 8 A8.000 Selvinspektion A8.1 A8.010 Generelt A8.1 A8.020 Kvalitetsstyring A8.2 A8.030 Donoregnethed A8.9 A8.040 Tapning af blod A8.11 A8.050 Fremstilling af blodkomponenter A8.12 A8.060 Undersøgelser af donorblod A8.14 A8.900 Apparaturoversigt A8.16 APPENDIKS 9 A9.000 Kvalitetskontrol af blodkomponenter A9.1 A9.100 Indledning A9.1 A9.200 Deklaration A9.1 A.9.300 Validering af fremstillingsmetoder og fastlæggelse af specifikationer A9.2 A9.400 Valideringsmasterplan A9.3 A9.500 Den løbende kvalitets- og procedurekontrol A9.3 A9.600 Afvigelsessrapporter A9.3 A9.700 Minimale kvalitetskontrolparametre på blodkomponenter A9.4 APPENDIKS 10 A10.000 Eksempler på information ved typeskift A10.1 A10.100 Erytrocytter A10.1 A10.200 Plasma A10.1 APPENDIKS 11 A11.000 Rekommandationer for anvendelse af leukocytdepleterede blodkomponenter A11.1 A11.100 Generelt A11.1 A11.200 Indikationer for anvendelse af leukocytdepleterede blodkomponenter A11.1 © 1994-2004 Dansk Selskab for Klinisk Immunologi
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TMS.2.3.2004

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