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
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