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TOPIC 2 SESSION 6: Reporting Requirements in Special Situations in the Post-authorisation Phase and Case Studies
Session Chair(s)
Gaby L. Danan, MD, PhD
Pharmacovigilance Expert, GLD, France
Phil Tregunno
Deputy Director - Patient Safety Monitoring, Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
Speaker(s)
Reporting Requirements in Special Situations in the Post-authorisation Phase and Case Studies
Sarah Vaughan
Head of Vigilance Operations, Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
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