Medical Devices 2011 - Webinar on Medical Device Tracking - Medical Devices Webinar By ComplianceOnline

Why Should You Attend:
The Food and Drug Administration Modernization Act (FDAMA) requires that manufacturers track certain devices when the agency orders them to do so. Tracking is intended to facilitate notification and recall in the event a device presents a serious risk to health that requires prompt attention. The tracking provisions enacted by SMDA in section 519(e) required mandatory tracking even if FDA did not issue an order.

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