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Zdrowie i gospodarka · 01/04/2024

FDA Finalizes Guidance for Electronic Submission of IND Safety Reports

The Food and Drug Administration (FDA) has released a final guidance outlining the electronic format requirements for submitting investigational new drug application (IND) safety reports, which will become effective 24 months after publication on April 1, 2026.

Source: Federal Register — Food and Drug AdministrationOpen original release →