BN Business News
Add your company to Business Communicator →

Zdrowie i gospodarka · 21.10.1998

Antibody to Human T-Cell Lymphotropic Virus Type II (HTLV-II) Reference Panel 1; Availability

The Food and Drug Administration (FDA) is announcing the availability of a new FDA reference panel for tests intended to detect antibody to human T-cell lymphotropic virus Type II (HTLV-II Reference Panel 1). The HTLV-II Reference Panel 1 is used for the qualitative and semiquantitative evaluation of in vitro tests to detect antibody to HTLV-II in human serum or plasma. The HTLV-II Reference Panel 1 is designed to provide a release criterion for lots of HTLV-II antibody detection kits produced by licensed manufacturers of such tests and should not be used for experimental or other reference purposes.

Source: Federal Register — Food and Drug AdministrationOpen original release →