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Guidance Documents/Guidance-Document/Validation of Certain In Vitro Diagnostic Devices for Emerging Pathogens During a Section 564 Declared Emergency: Draft Guidance for Industry and Food and Drug Administration Staff

Validation of Certain In Vitro Diagnostic Devices for Emerging Pathogens During a Section 564 Declared Emergency: Draft Guidance for Industry and Food and Drug Administration Staff

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

January 6, 2025

February 12, 2025

Center for Devices and Radiological Health

3594dad0-5e3f-41d0-8d24-8085dde76c83

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