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 4: Key elements of Periodic Safety Update Reports (PSURs)

Speaker(s)

Key elements of Periodic Safety Update Reports (PSURs)

Louise Larham

Amgen Limited, United Kingdom

EU Regional Safety Lead, Global Patient Safety

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

Topic 2 Session 4: Key elements of Periodic Safety Update Reports (PSURs)

Speaker(s)

Key elements of Periodic Safety Update Reports (PSURs)

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