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Holiday Inn London Kensington Forum

Nov 14, 2016 8:00 AM - Nov 18, 2016 1:30 PM

97 Cromwell Road, London, SW7 4DN, United Kingdom

Joint MHRA/DIA Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing

The 5 days of training include a comprehensive overview of the core processes and systems in place and the latest news on the international harmonisation and standardisation activities in pharmacovigilance.

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Topic 2 Session 5: Expedited Reporting Requirements in the Post-authorisation Phase and Case Studies

Speaker(s)

Gaby L. Danan, MD, PhD

Expedited Reporting Requirements in the Post-authorisation Phase and Case Studies

Gaby L. Danan, MD, PhD

GLD, France

Pharmacovigilance Expert

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