FDA Adverse Event Reporting System (FAERS)
OBJECTIVES
The course intends to provide you with an overview of the FAERS database, particularly :
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The FDA Adverse Event Reporting System (FAERS)
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Access to the system
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Uses of FAERS
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Interpretation of statistical safety signals
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Strengths and Limitations of the FAERS Database
FAERS, database, limitations, strengths, FDA
LEARNING OUTCOMES
At the end of the course, you should be able to :
Describe the FAERS database
Explain how to access the FAERS database
Enumerate the uses of the FAERS database
Interpret safety signals derived from the FAERS database
Describe strengths of the FAERS database
Describe the limitations of the FAERS database
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150 minutes |
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Online based learning |
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English language |
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Certificate of Achievement |
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250 € / $270 |
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REGISTER NOW
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AUTHORS
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Dr. Maribel Salas
Head of Epidemiology and Head of Cardiovascular, Clinical Safety and Pharmacovigilance
Daiichi-Sankyo
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Nasop Experts Group
ISoP's North American chapter
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This short course has been added to your Study List:
FDA Adverse Event Reporting System (FAERS)
Please note that this short course is currently in update.
It will be available within 15 working days.
This short course has been added to your Study List:
FDA Adverse Event Reporting System (FAERS)
COMPANIES OFFER
Short courses can be included in a training package for your team!
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