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FDA Adverse Event Reporting System (FAERS)


Eu2P Short Course: FDA Adverse Event Reporting System (FAERS)

OBJECTIVES

The course intends to provide you with an overview of the FAERS database, particularly :

  • The FDA Adverse Event Reporting System (FAERS)
  • Access to the system
  • Uses of FAERS
  • Interpretation of statistical safety signals
  • 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

 

150 minutes
Online based learning
English language
Certificate of Achievement
250 € / $290
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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




COMPANIES OFFER

Short courses can be included in a training package for your team!


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