supply of anti hcv rapid test/crp tests/anti hbc total elisa test/atex agglutination. , srphc82670065-anti hcv rapid test: 1. should be 3rd generation. 2. based on immunochrom atography / immunofiltration for the qualitative detection of antibodies specific to hcv in human ser um, plasma, or whole blood. 3. should be solid phase / particle coated with recombinant and / or synt hetic peptide antigens for core, ns3, ns 4, and ns5. 4. should have in built quality control band or do t 5. should have short interpretation time not more than 30 minutes 6. should have specificity greate r than and equal to 98% and sensitivity of greater than and equal to99% 7. must be evaluated and ap proved by nib 8. original technical data sheet should be provided with each kit. 9. the kit should hav e minimum shelf life of 60% or 12 months (whichever is more) at the time of delivery to consignee unit :test ] , srphc82670100-crp tests - immunoturbidmetric assay: 1. compatibility: reagents must be f ully compatible with beckman coulter au480 automated clinical chemistry analyser. 2. method: immun oturbidimetric or latexenhanced immunoturbidimetric method. 3. reagent type: ready-to-use, liquidst able r1 and r2 reagents. 4. measuring range: minimum 5.00?200 mg/l. 5. stability: on-board stability sh ould be greater than and equal to 30 days, shelf life greater than and equal to 12?18 months. 6. cal ibration: dedicated crp calibrators (1-point or 2-pint or multi-point) must be provided. 7. controls: n ormal and high crp controls must be supplied or specified as compatible. 8. accuracy: results tracea ble to ifcc/crm 470 reference standard. precision: cv less than and equal to 5% (within-run) and less than and equal to 7% (between-run). 9.loading: barcode-enabled, directly loadable on au480 withou t adapters. 10. labeling: each pack must indicate lot number, expiry date, storage conditions, and ana lyser compatibility. 11. storage: reagents must be stored at 2?8 degree celsius. 12. documentation: m ust have ifu, msds, coa, ce-ivd/iso documentation. 13. support: supplier must provide technical suppor t, troubleshooting, and replacement of defective or unstable lots. 14. compliance: manufacturer au thorization letter and declaration of compatibility with beckman coulter au480 must be submitted. ] , srphc82670035-anti hbc total elisa test--96 tests/kit unit:test ] , srphc82670105-crp-latex agglutination assay (reagent for semi auto analysers) unit:test ]