• Full range of Pharmacovigilance services
  • All day L-QPPV contact (24h/7)
  • Reporting in the Eudravigilance system
  • Acceptance, processing and reporting of individual case reports (regarding adverse reactions) related to medicinal products (Individual Case Safety Report)to the relevant authorities
  • Monitoring websites of Polish and international institutions - (Registration Agency, Main Pharmaceutical Inspector, MoH) regarding information concerning PHV cases.
  • Archiving of documents, reports, magazine printouts, single application forms in accordance
  • with legal requirements and procedures in electronic and paper versions
  • Monitoring of Polish medical literature according to the requirements of Good Pharmacovigilance Practice guidelines
  • PV training for contractors