Guidance for industry : revised recommendations regarding invalidation of test results of licensed and 510(k) cleared bloodborne pathogen assays used to test donors.

Other author Center for Biologics Evaluation and Research (U.S.)
Format Electronic
Publication InfoRockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001]
Descriptioni, 5 p. : digital, PDF file
Supplemental Contenthttps://purl.fdlp.gov/GPO/LPS113257
Subjects

Portion of title Revised recommendations regarding invalidation of test results of licensed and 510(k) cleared bloodborne pathogen assays used to test donors
General noteTitle from PDF title page (viewed on May 29, 2009).
General note"July 2001".
General noteGPO Cataloging Record Distribution Program (CRDP).
Bibliography noteIncludes bibliographical references (p. 5).
Technical detailsMode of access: Internet at the FDA CBER web site. Address as of 5/29/09: http://www.fda.gov/cber/gdlns/bldbrn.pdf ; current access is available via PURL.
GPO item number0499-T-02 (online)
Govt. docs number HE 20.4802:IN 8/3

Availability

Library Location Call Number Status Item Actions
Electronic Resources Access Content Online ✔ Available