Use of Public Human Genetic Variant Databases to Support Clinical Validity for Genetic and Genomic-B...
Use of Public Human Genetic Variant Databases to Support Clinical Validity for Genetic and Genomic-B...
Use of Public Human Genetic Variant Databases to Support Clinical Validity for Genetic and Genomic-Based In Vitro Diagnostics
About this item
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Author / Creator
Publisher
United Kingdom: Jenny Stanford Publishing
Journal title
Language
English
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Publication information
Publisher
United Kingdom: Jenny Stanford Publishing
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Scope and Contents
Contents
This chapter describes one part of Food and Drug Administration's (FDA) efforts to create a flexible and adaptive regulatory approach to the oversight of next generation sequencing (NGS)-based tests. The goal of this effort is to help ensure patients receive accurate, reliable, and clinically meaningful test results, while promoting innovation in t...
Alternative Titles
Full title
Use of Public Human Genetic Variant Databases to Support Clinical Validity for Genetic and Genomic-Based In Vitro Diagnostics
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Record Identifier
TN_cdi_proquest_ebookcentralchapters_30733439_100_566
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_ebookcentralchapters_30733439_100_566
Other Identifiers
ISBN
9814877468,9789814877466
DOI
10.1201/9781003298038-14
