FDA 483 OBSERVATION · #709 OF 1,000 MOST-CITED
Safety Reports - Non-Serious Events
FDA cited this observation 23 times across 23 firms in recent inspections. Below: how it breaks down by program area and fiscal year, and real examples of how FDA worded it on Form FDA 483.
How FDA worded it — real examples
Failure to report non-serious adverse events to the sponsor in accordance with the study protocol timetable for reporting.
Failure to report non-serious adverse events to the sponsor in accordance with the study protocol timetable for reporting.
Failure to report non-serious adverse events to the sponsor in accordance with the study protocol timetable for reporting.
Failure to report non-serious adverse events to the sponsor in accordance with the study protocol timetable for reporting.
Failure to report non-serious adverse events to the sponsor in accordance with the study protocol timetable for reporting.
Failure to report non-serious adverse events to the sponsor in accordance with the study protocol timetable for reporting.
Related SPEQ references
Where to read the requirements behind this observation area on SPEQ. These are SPEQ's topic and audience pages — not an FDA classification of the citation.
Examples are a representative sample of FDA's published inspection observations. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.
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