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FORM FDA 3500A SUPPLEMENT
Manufacturers must prepare and submit a complete. Form FDA 3500A for each suspect device. Each Form FDA 3500A will be given a separate. Manufacturer Report
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Case Report Form Templates ICTR UWMadison
Case Report Form (CRF)/Source Document templates were created for University of Wisconsin-Madison researchers. These templates are consistent with the FDA
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Guidelines To Writing A Clinical Case Report - PMC
WHAT IS A CLINICAL CASE REPORT? A case report is a detailed report of the symptoms, signs, diagnosis, treatment, and follow-up of an individual patient.
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