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Joint DIA/EFGCP Pharmacovigilance Audit and Inspection Workshop - Opportunities for Patient Safety

1 October 2010, London, United Kingdom


Introduction
Audit and inspection findings related to:
• Management of individual case safety reports such as assessment of case validity, lack of efficacy, information derived from the Internet
• Record retention and storage, paper versus electronic records
• Pharmacovigilance quality system, structure, documentation, Detailed Description of Pharmacovigilance Systems (DDPS) updates, role of European Qualified Person for Pharmacovigilance (QPPV)
• Reporting of inspection findings, assessment against internal/external references, interpretation of regulatory requirements, consistency across inspections, options for dialogue and escalation
Venue
DE VERE Venues Canary Wharf

DE VERE Venues Canary Wharf, London, United Kingdom

Organised by
DIA in Europe
Contact information
Mr Michael Hediger
Contact us by email

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