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USFDA’s Med Dev Guidance: The Q-Submission Program & Electronic Submission Template for Medical Device Q-Submissions
As medical technology advances, the FDA’s regulatory frameworks continue evolving to ensure timely, safe, and effective device...

Sharan Murugan
May 302 min read
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USFDA MD Guidance: AST System Devices, Technical Considerations & Electronic Submission Template
Recently (29th September 2023) the U.S. Food and Drug Administration (FDA) Center for Devices and Radiological Health released multiple...

Sharan Murugan
Oct 2, 20232 min read
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