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WEBINAR FDA Discusses Sentinel Initiative May 20, 2009 12:00 PM1:30 PM EDT 11:00 AM12:30 PM CDT 10:00 AM11:30 AM MDT 9:00 AM10:30 AM PDT STANDARD MEMBER $250 FEATURED FDA PRESENTERS BRAM HARLEM, PhD,
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What is fda discusses sentinel?
FDA Discusses Sentinel is a program established by the U.S. Food and Drug Administration (FDA) to monitor the safety of medical products after they have been approved for use.
Who is required to file fda discusses sentinel?
Manufacturers, importers, and distributors of medical products are required to file reports with FDA Discusses Sentinel.
How to fill out fda discusses sentinel?
To fill out FDA Discusses Sentinel, companies must submit relevant safety information about their medical products using the online reporting system provided by the FDA.
What is the purpose of fda discusses sentinel?
The purpose of FDA Discusses Sentinel is to identify and address potential safety concerns related to medical products and to ensure the continued safety of patients.
What information must be reported on fda discusses sentinel?
Information such as adverse events, product defects, and other safety issues related to medical products must be reported on FDA Discusses Sentinel.
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