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Electronic Submission of Adverse Event Reports to FDA FAERS
The purpose of these public meetings is to provide the pharmaceutical industry and other interested parties with information on the plans, progress, and technical specifications to upgrade electronic submission standards for the premarket and postmarket safety surveillance programs managed by CDER and CBER
Apr 28, 2019
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1.9K views · 18 shares | Ever wonder what it takes to take a drug from discovery to market? Dr. Theresa Strong discusses the stages of development and how you can help not only get drugs through clinical trials but also with the approval process. You can watch the entire presentation that includes information on each clinical trial here: https://www.fpwr.org/blog/2019-pws-clinical-trials-panel-video | The Foundation for Prader-Willi Research | Facebook
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