We keep asking ourselves how do we tackle benefit-risk assessment using advanced structured approaches in real life. It is difficult, especially when we know that benefit-risk balance is not constant over time. How should we approach it to begin with, and how do we update it when new evidence comes into the equations? Dr Kaatje Bollaerts (P-95) and I are chairing the next DIA Pharmacovigilance Workshop to discuss this topic.
Share your experience in this area so we can discuss this topic further, and hopefully take the harmonisation of structured benefit-risk assessment to the next level!