How often must manufacturers submit adverse event reports to the FDA?

Manufacturers are required to submit adverse event reports to the FDA promptly, traditionally within 30 days of becoming aware of the adverse event. This requirement ensures that the FDA is kept informed about potential safety issues related to medical devices, allowing for timely risk assessments and regulatory action if necessary. The 30-day timeframe is crucial as it helps to facilitate swift investigations and responses to possible safety concerns, ultimately protecting public health. Regularly submitting these reports aids in monitoring the safety and efficacy of devices in the market and contributes to overall surveillance activities.