Voluntary Malfunction Summary Reporting (VMSR) Program for Manufacturers: Guidance for Industry and Food and Drug Administration Staff

Information

Type

Guidance

Regulated products

Biologics, Medical Devices

Published

August 29, 2024

Last updated

August 28, 2024

Description

A guidance document outlining the Voluntary Malfunction Summary Reporting (VMSR) Program for Manufacturers, providing guidance for industry and FDA staff.

Organization

Country / Region

United States

License

Other (Public Domain)

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