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Overview of the FDA Submission Process Nina Hunter, PhD FDA/CDR/OR/DID NCI SIR Workshop on Federal Resources to Accelerate Commercialization May 7, 2013, Office of Medical Products and Tobacco Center
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Healthcare professionals: Medical practitioners, doctors, and researchers who are involved in activities regulated by the FDA may need to fill out the overview of form FDA. This could include clinical trials, drug approvals, or medical device applications.
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Form FDA is a form used by medical product manufacturers to report adverse events or potential safety concerns to the Food and Drug Administration (FDA).
Medical product manufacturers are required to file the overview of form FDA.
The form can be filled out online on the FDA's website or submitted in paper form. It requires information about the product, the adverse event, and contact information for the manufacturer.
The purpose of the overview of form FDA is to allow the FDA to monitor the safety of medical products on the market.
Information such as the product name, manufacturer, adverse event details, and contact information must be reported on the overview of form FDA.
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