The FDA approves Roche’s (OTCQX:RHHBY) cobas HIV-1/HIV-2 Qualitative Test for the qualitative detection and differentiation of HIV-1 and HIV-2 RNA in serum or plasma. The nucleic acid amplification assay is performed on the fully automated cobas 6800/8800 systems in the U.S.
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.