Iggea can support your company to ensure that Pharmacovigilance systems are properly established. We are here to assist you in building or upgrading existing systems to ensure compliance with the new pharmacovigilance requirements.

Our pharmacovigilance services include:

  • Writing and Review of Pharmacovigilance SOPs
  • EU QPPV  Services
  • Local QPPV
  • Writing Risk Management Plan (RMP)
  • Compilation and update of the DSUR
  • Compilation and maintenance of the PSMF
  • Local literature searching
  • Interaction with Eudravigilance database

Iggea’s services vary from full coverage and provision of safety operations to specialist consulting.