In Vitro Automated Reagents Salient Characteristics.docx
DOCX document 19 KB Posted
- Attached to
- Ortho Vision analyzer Reagents and Supplies
- Solicitation number
- W81K02-20-Q-0174
- Issued by
-
Department of the Army Medical Command
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Other files
| File | Type | Posted |
|---|---|---|
| Reagent List.doc | DOC document | |
| Statement of Work In Vitro Reagents.doc | DOC document |
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In Vitro (traditional and automated) Reagents/ Supply Salient Characteristics
1. CHARACTERISTICS
a. Must be compatible with use on Government owned analyzer (Ortho Diagnostics ProVue Analyzer)
b. All reagents must be made in the USA per FDA regulations/policy
c. Must be able to provide 100% of the reagents listed on reagent list.
d. Provide a minimum of 3 panels for antibody ID on bench and automated platform
e. Must have a complete line of antigen typing antisera (Kidd, Duffy, Rh, Lewis, MNSs)
f. Manufacturer Quality Controls available for automation and bench testing
g. Must have capability to supply gel reagents and supplies and testing on gel automated platforms, gel back-up, AND traditional tube/ bench testing
h. All reagents must be FDA approved
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