Training sessions on the following topics:

  • “Regulatory Specialist for Medical Products”
  • “Pharmacovigilance Specialist. Drug Safety Monitoring”
  • “Clinical Trials of Medicinal Products. ICH GCP Guidelines”
  • “Introduction to GMP. Good Manufacturing Practice Standards for Non-Manufacturing Organizations”
  • “Quality System of Medicinal Products”

More detailed information is available on the page – Training Center