Requests for Feedback and Meetings for Medical Device Submissions: The Q-Submission Program - Draft Guidance for Industry and Food and Drug Administration Staff

Information

Type

Guidance

Regulated products

Biologics, Medical Devices

Topics

Administrative / Procedural, Premarket

Published

March 15, 2024

Last updated

March 14, 2024

Description

Draft guidance document on Q-Submission Program for medical device submissions, covering administrative/procedural and premarket topics.

Organization

Country / Region

United States

License

Other (Public Domain)

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