CONSCIOUS I Curriculum Chapter 13: Adverse events and reporting responsibilities

Category

  • Clinical Trial Management
webinar
  • Topic: Pharmacovigilance
  • Short Description: The importance of pharmacovigilange throughout a product’s life cycle; European Union (EU) pharmacovigilance system; obligation of reporting to EudroVigilance in interventional clinical trials (who and what); types of adverse events
  • Provider: Conscious I consortium
  • Level: Beginner
  • Language: English
  • Cost: Free
  • Format: On-line modules
  • Duration: Unknown
  • Certificate: No
  • Link
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