Our colleagues are able to provide wide range of adverse drug reaction monitoring and reporting activities in compliance with international requirements, solving issues on a daily basis emerging in this field and answering queries.

  • monitoring up-to-date laws and legislations
  • literature screening
  • preparation of periodic safety update reports
  • full support of clinical trial adverse reaction reporting obligation
  • pharmacoepidemiology studies
  • training and advanced training in pharmacovigilance


Go to Quality Management