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INOPP ForumMedical Device Vigilance (Materiovigilance): Global Device Vigilance RequirementsUnited States

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United States

Device Vigilance Requirements in the United States

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Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic ActBy VigiServe Admin0 Replies · 87 ViewsLast post: 2 years ago · VigiServe Admin

2 years ago
VigiServe Admin

Voluntary Malfunction Summary Reporting (VMSR)By VigiServe Admin0 Replies · 133 ViewsLast post: 3 years ago · VigiServe Admin

3 years ago
VigiServe Admin

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