Tables
Table 2.1List of some key inspection/licensing/accreditation/certification standardsTable III.ITotal blood volume (TBV) and extra-corporeal blood volume (ECV)Table IV.ICitrate anticoagulantsTable 8.1Whole Blood, Leucocyte Depleted – additional testsTable 8.2Red Cells, Leucocyte Depleted – additional testsTable 8.3Red Cells in Additive Solution, Leucocyte Depleted – additional testsTable 8.4Red Cells, Washed, Leucocyte Depleted – additional testsTable 8.5Red Cells, Thawed and Washed, Leucocyte Depleted – additional testsTable 8.6Platelets, Pooled, Buffy Coat Derived, Leucocyte Depleted – additional testsTable 8.7Platelets, Apheresis, Leucocyte Depleted – additional testsTable 8.8Platelets, Suspended in Platelet Additive Solution, Leucocyte Depleted – additional testsTable 8.9Granulocytes, Apheresis – additional testsTable 8.10Fresh Frozen Plasma, Leucocyte Depleted – additional testsTable 8.11Fresh Frozen Plasma, Methylene Blue Treated and Removed, Leucocyte Depleted – additional testsTable 8.12Cryoprecipitate, Leucocyte Depleted – additional testsTable 8.13Plasma, Cryoprecipitate Depleted, Leucocyte Depleted – additional testsTable 8.14Red Cells for Intrauterine Transfusion (IUT), Leucocyte Depleted – additional testsTable 8.15Whole Blood for Exchange Transfusion, Leucocyte Depleted – additional testsTable 8.16Red Cells for Exchange Transfusion, Leucocyte Depleted – additional testsTable 8.17Red Cells for Neonates and Infants, Leucocyte Depleted – additional testsTable 8.18Red Cells in Additive Solution for Neonates and Infants, Leucocyte Depleted – additional testsTable 8.19Fresh Frozen Plasma, Neonatal Use, Methylene Blue Treated and Removed, Leucocyte Depleted – additional testsTable 8.20Cryoprecipitate, Methylene Blue Treated and Removed, Leucocyte Depleted – additional testsTable 8.21Platelets for IUT, Leucocyte Depleted – additional testsTable 8.22Platelets for Neonatal Use, Leucocyte Depleted – additional testsTable 8.23Red cell componentsTable 8.24Platelet and granulocyte componentsTable 8.25Plasma componentsTable 8.26Neonatal and infant red cell componentsTable 8.27Neonatal and infant platelet componentsTable 8.28Neonatal and infant plasma componentsTable 8.29Blood components suitable for use in intrauterine and exchange transfusion and neonates and infants under one year, specific requirementsTable 9.1Testing of novel componentsTable 9.2Evaluation of new red cell components for transfusion: recommended testsTable 9.3In vitro assessmentTable 9.4Evaluation of new platelet components for transfusionTable 9.5Evaluation of novel plasma componentsTable 9.6Generic flowchart of apheresis equipment acceptanceTable 9.7Summary of testing numbers required for evaluations and validationsTable 12.1Label colour codingTable 12.2Grading system for serological testsTable 12.3Requirements for conventional blood typing reagentsTable 12.4Chequerboard test formatTable 12.5Complement C3 and C4 activationTable 13.1Minimum release criteria for blood products with antibodies of probable clinical significanceTable 13.2Test monitor red cell samplesTable 14.1Timing of pre-transfusion samplesTable 14.2Suggested maximum storage time of samplesTable 14.3Controls for manual and automated ABO and D groupingTable 15.1Dilution of UK reference reagentTable 15.2HLA antigens that are defined by serological typingTable 15.3Characterization of HLA-specific antibodiesTable 16.1Current nomenclature for human neutrophil antigens and corresponding antibodiesTable 17.1Current HPA nomenclature for platelet-specific alloantigen and alloantibody specificitiesTable 22.1Microbiological testing for tissue donorsTable 23.1Temperature/time relationships for banked tissuesTable 23.2Air classification system for manufacture of sterile medicinal productsTable 23.3Comparison of British, European and American classificationsTable 23.4Microbiological monitoring of controlled work areasTable 23.5Ethylene oxide and ethylene chlorohydrin residue levelsTable 23.6Minimum donor/recipient data set to be keptTable 24.1Requirements for the timing of testingTable 24.2Label content adapted from FACT-JACIETable 24.3Label content for HPC-C adapted from NETCORD-FACTTable 25.1Centre codes and namesTable 25.2aBlood group classificationsTable 25.2bBlood group and donation use limitationsTable 25.2cBlood group and donation use label textTable 25.3Historic blood group classifications (only for use on 'Use in emergency only' labels)Table 25.4Manufacturers'codesTable 26.1Statements of product statusTable 26.2Glossary: uniform labelling of human tissue productsTable 27.1Envelope definitionTable 27.2Message protocol numbersTable 27.3Message protocol 000001: blood component dispatch information: administrationlineTable 27.4Message protocol 000001: blood component dispatch information: dispatch lineTable 27.5Message protocol 000001: blood component dispatch information.Field 10: Red cell phenotype field – antigen codesTable 27.6Message protocol 000001: blood component dispatch information.Field 14: Platelet-specific phenotypeTable 27.7Message protocol 000002: blood derivative dispatch information: administrationlineTable 27.8Message protocol 000002: blood derivative dispatch information: dispatch lineTable 27.9Message protocol 000003: reagent dispatch information: administrationlineTable 27.10Message protocol 000003: reagent dispatch information: dispatch lineTable 27.11Message protocol 000004: blood component dispatch acknowledgement: administrationlineTable 27.12Message protocol 000004: blood component dispatch acknowledgement: dispatch lineTable 27.13Message protocol 000005: blood component fate information: data lineTable 27.14Message protocol 000005: blood component fate information. Field 8: wasted classification codeTable A1.1Serological, virological and other preparationsTable A1.2Coagulation preparations: WHO International StandardsTable A1.3Coagulation preparations: British StandardsTable A2.1Mapping from characters to ISO 7064 check valuesTable A2.2Example of displayed numbers