Corpus Medica can offer full Pharmacovigilance support in all three Baltic countries, Lithuania, Latvia and Estonia.  

Pharmacovigilance service including:

  • EU Qualified person for Pharmacovigilance (QP for PV)
  • Registration of the Marketing authorisation holder (MAH) in EudraVigilance system
  • Safety report formulation and transmission via the EudraVigilance system
  • Work with EudraVigilance Post-Authorisation Module (xEVMPD) Literature Searching Preparation of Periodic Safety Update Reports (PSUR)
  • Preparation of Risk Management Plan (RMP); Pharmacovigilance system site master file development (PSMF)
  • Pharmacovigilance Trainings