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Initial Build | SE 1/31 |
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Staff Review | Suzanne Wood |
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Approval Status | |
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Description
Determination of whether or not event was reported to the FDA’s voluntary reporting system, MedWatch.
On-Screen Instructions
Note: MedWatch is the Food and Drug Administration’s (FDA’s) voluntary reporting system for an adverse events associated with the use of a medical product.
Field Type
Include Page |
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| Radio button excerpt |
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| Radio button excerpt |
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Responses
Guide for Use
Include Page |
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| No additional guidance excerpt |
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| No additional guidance excerpt |
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