Date

Tuesday, 21 November 2023, 09:30 (CET) - 17:00 (CET)

Location

European Medicines Agency, Amsterdam, the Netherlands

Event summary

Key topics:

  • EudraVigilance data protection activities
  • Substance, product, organisation and referential (SPOR) data
  • Revision of ICH- E2D
  • ICSRs quality control
  • Pharmacovigilance Inspections
  • EudraVigilance Operational activities

Documents

Registration

Please follow the link to register, or use the form above:

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