TMS.2.3.2004

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ii Transfusionsmedicinske Standarder. Version 2.3 3.080 Produktidentifikation og -sporbarhed 3.5 3.090 Processtyring 3.5 3.100 Inspektion og prøvning 3.6 3.110 Styring af inspektions-, måle- og prøvningsudstyr 3.7 3.120 Inspektions- og prøvningsstatus 3.7 3.130 Styring af afvigende produkter 3.7 3.140 Korrigerende og forebyggende handlinger 3.8 3.150 Håndtering, opbevaring, emballering, bevarelse og levering 3.8 3.160 Styring af registreringer vedrørende kvalitet 3.8 3.170 Selvinspektion (intern kvalitetsaudit) 3.9 3.180 Uddannelse/træning 3.9 3.190 Service 3.10 3.200 Statistiske metoder 3.10 KAPITEL 4 4.000 Bloddonorer 4.1 4.100 Definition 4.1 4.200 Oplysninger til donor 4.1 4.300 Oplysninger fra donor 4.2 4.400 Registrering af bloddonorer 4.2 4.500 Generelle alders- og helbredskriterier 4.3 4.600 Aferese af bloddonorer 4.4 4.700 Overflytning af bloddonorer 4.4 KAPITEL 5 5.000 Blodtapning: generelle regler 5.1 5.100 Almindelig tapning 5.1 5.200 Aferesetapning 5.1 5.300 Blodtapningernes hyppighed og størrelse: almindelig tapning 5.1 © 1994-2004 Dansk Selskab for Klinisk Immunologi
Transfusionsmedicinske Standarder. Version 2.3 iii 5.400 Blodtapningernes hyppighed og størrelse: plasmaferese- og cytaferesetapning 5.2 5.500 Registrering af blodtapninger 5.3 KAPITEL 6 6.000 Tapning af bloddonorer 6.1 6.100 Tapning i blodbanker eller ved mobile blodtapninger 6.1 6.200 Generelle regler 6.1 6.300 Sikkerhedsforanstaltninger 6.2 6.400 Plasma- og cytaferesetapning, specielt 6.5 KAPITEL 7 7.000 Blodtypebestemmelse af bloddonorer - minimumskrav 7.1 7.100 Indledning 7.1 7.200 Alment 7.1 7.300 AB0 blodtypebestemmelse 7.1 7.400 RhD blodtypebestemmelse 7.2 7.500 Screentest for erytrocytantistoffer 7.2 7.600 Svarafgivelse 7.2 KAPITEL 8 8.000 Fremstilling af blodkomponenter 8.1 8.100 God fremstillingspraksis 8.1 8.200 Selvinspektion 8.1 8.300 Lokaler 8.1 8.400 Udstyr 8.2 8.500 Hygiejne 8.3 8.600 Emballage - Utensilier 8.4 8.700 Instruktioner 8.4 © 1994-2004 Dansk Selskab for Klinisk Immunologi
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TMS.2.3.2004

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