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Check with seller FDA Adverse Event Reporting System Florida City

Published date: May 13, 2021
  • Location: Florida City, Florida, United States

Clinical reviewers evaluate the reports in FAERS in the Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) to monitor products’ safety after the FDA approves them.


If a potential safety concern is discovered in FDA Adverse Event Reporting System (FAERS), further evaluation is performed. Based on the evaluation, FDA may take regulatory action(s) to improve product safety and protect public health.


Please visit our website: https://www.compliancequest.com/
Keywords: FDA Adverse Event Reporting System
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