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Guidance Documents/Guidance-Document/How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1): Guidance for Industry

How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1): Guidance for Industry

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

September 9, 1998

February 3, 2025

Center for Biologics Evaluation and Research

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