Tuesday, 22 April, 2025
1:40 pm - 3:10 pm
Mastering European regulatory timeline assumptions – a practical guide to elevate competitors’ analysis
An interactive session where the Lifescience Dynamics team will share its knowledge and experience in understanding and evaluating EU regulatory timelines
• An introduction to EU regulatory pathways including recent changes to MHRA approval timelines
• What are the critical differences between the FDA and EMA approval pathways?
• Interactive case studies on varying types of approval scenarios and what we can learn from them
Presented by Lifescience Dynamics