Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (home

About this role

The EU QPPV is responsible for:• The establishment and maintenance of a system which ensures that information about all suspected adverse reactions which are reported to the personnel of the Company, and to medical representatives, is collected and collated in order to be accessible at least at one

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• QPPV
• Pharmacovigilance-Specialist
• Drug-Safety-Specialist
• Regulatory-Affairs-Specialist
• Medical-Affairs-Specialist
• Pharmacovigilance-(PV)
• Pharmacovigilance-Manager
• Pharmacovigilance-Management

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