Electronic Submission of Adverse Event Reports to FAERS using ICH E2B(R3) Standards - Oct. 11, 2019

  Рет қаралды 3,814

U.S. Food and Drug Administration

U.S. Food and Drug Administration

Күн бұрын

Suranjan De from CDER’s Office of Surveillance & Epidemiology discusses plans, progress, and technical specifications on enhancements to electronic submission of premarket and post-market Individual Case Safety Reports (ICSRs) in FAERS using ICH E2B(R3) standards.
Find more information at www.fda.gov/dr...
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