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Holiday Inn London Kensington Forum

Feb 27, 2017 8:00 AM - Mar 03, 2017 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.

Back to Agenda

Topic 2 Session 6: Reporting Requirements in Special Situations in the Post-authorisation Phase and Case Studies

Speaker(s)

Sarah Vaughan

Reporting Requirements in Special Situations in the Post-authorisation Phase and Case Studies

Sarah Vaughan

Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom

Head of Vigilance Operations

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