First Accredited Diploma in Pharmacovigilance for the Middle East

Do you need detailed information about the European Pharmacovigilance framework in order to understand and implement the
new Common Arab Guidelines in Pharmacovigilance in your country? We would like to invite you to join our 12 live and recorded
webcasts, where European and Middle East experts will inform you of the concepts and challenges in drug safety that you need to
remain compliant with your current PV legislation.
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You will meet our experts in a virtual conference room. Each meeting will be a two-hour live webcast, delivering the information
with supporting slides (also for your personal download). Your practical questions will be addressed directly via the chat function
coordinated by the meeting chairperson. The webcast series will start in February 2018 and will be completed after 6 months.
Dates and time will be announced one month prior to the webcast.

Themen

- Qualified person for pharmacovigilance (QPPV)
- Pharmacovigilance system master file (PSMF) and PSSF
- Drug adverse reactions and signal management
- Risk management plan (RMP) and risk management system
- Periodic safety update reports (PSUR)
- Pharmacovigilance inspection and audit readiness