Research Catalog

Title

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

Publication

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001]

Details

Additional Authors

Center for Biologics Evaluation and Research (U.S.)

Description

i, 5 p. : digital, PDF file.

Alternative Title

Revised recommendations regarding invalidation of test results of licensed and 510(k) cleared bloodborne pathogen assays used to test donors

Subject

• Microbiological assay > Government policy > United States
• Blood donors > Government policy > United States

Note

• Title from PDF title page (viewed on May 29, 2009).
• "July 2001".

Bibliography (note)

• Includes bibliographical references (p. 5).

System Details (note)

• Mode 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.

Call Number

GPO Internet HE 20.4802:IN 8/3

OCLC

362359064

Title

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

Imprint

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001]

System Details

Mode 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.

Bibliography

Includes bibliographical references (p. 5).

Connect to:

http://purl.access.gpo.gov/GPO/LPS113257

Added Author

Center for Biologics Evaluation and Research (U.S.)

Gpo Item No.

0499-T-02 (online)

Sudoc No.

HE 20.4802:IN 8/3

Research Call Number

GPO Internet HE 20.4802:IN 8/3