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Business · 20/05/2021

FDA Announces Draft Guidance on Waivers of Signature Requirement for Clinical Trial Investigators

The Food and Drug Administration (FDA) has released a draft guidance document that partially revises its previous guidance on clinical trial investigators, explaining the agency's current thinking on waivers of the signature requirement for Form FDA 1572, a critical form used in clinical trials.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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