Kingyin Lee
Head of Clinical Trials MHRA
Seminars
Wednesday 11th November 2026
Panel Discussion: Sharing Regulatory Navigation Strategies Across Global Agencies to Reduce Uncertainty & Accelerate Clinical Progression
1:45 pm
- Benchmarking regulatory pathways used across FDA, EMA & national authorities to clarify expectations and reduce trial approval uncertainty
- Comparing real-world regulatory interactions including key questions, feedback loops & submission strategies to strengthen future applications
- Identifying common pitfalls in CMC, trial design & product characterisation to proactively mitigate delays in regulatory approval processes
