13th Annual Outsourcing in Clinical Trials: Medical Devices Europe 2025
Talk
Medical device development roadmap: strategic decision-making on the path to market
Tue, Jan 28, 2025 · 4:30–5:00 PM CET Holiday Inn Munich City Centre
About this session
- Examine critical regulatory pathways, with strategic insights for achieving market clearance/approval in the US and EU
- Present streamlined approaches for planning and designing effective clinical studies, highlighting the benefits of budgeting early
- Discuss efficient processes for regulatory submissions and applications, from clinical study conduct to market clearance/approval
