Guidance for industry in the manufacture and clinical evaluation of in vitro tests to detect nucleic acid sequences of human immunodeficiency viruses types 1 and 2.
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| Format: | Government Document eBook |
| Language: | English |
| Published: |
Rockville, MD :
U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research,
[1999]
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| Subjects: | |
| Online Access: | https://purl.fdlp.gov/GPO/LPS113528 |
| Item Description: | Title from PDF title page (viewed on June 5, 2009). "December 1999". Electronic resource. |
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| Physical Description: | i, 22 pages : digital, PDF file. |
| Format: | Mode of access: Internet at the FDA web site. Address as of 6/5/09: http://www.fda.gov/downloads/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/Guidances/Blood/ucm080790.pdf ; current access is available via PURL. |
| Bibliography: | Includes bibliographical references (page 20). |