MedWatch Reporting Form 3500 (Voluntary Adverse Event Reporting Form) |
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MedWatch Reporting Form 3500A (Mandatory Adverse Event Reporting Form) For use by: IND Reporters, manufacturers, distributors, importers, user facilities personnel) |
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Medical Device Reporting Annual User Facility Report - Form FDA3419* |
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Medical Device Reporting Baseline Report - Form FDA3417* | ![]() |
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*These reports can be filled in on your PC. You may then print them out and mail to FDA
Updated April 1, 2008
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