FDA-IN VITRO DIAG Establishing the Performance Characteristics of In Vitro Diagnostic Devices for the Detection or Detection and Differentiation of Human Papillomaviruses - Guidance for Industry and Food and Drug Administration Staff

FDA-IN VITRO DIAG - 2017 EDITION - CURRENT
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Establishing the Performance Characteristics of In Vitro Diagnostic Devices for the Detection or Detection and Differentiation of Human Papillomaviruses - Guidance for Industry and Food and Drug Administration Staff


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Document Number

FDA-IN VITRO DIAG

Revision Level

2017 EDITION

Status

Current

Publication Date

Sept. 15, 2017

Page Count

41 pages