Lunch and Learn Series: Conducting Global Device Trials - San Francisco

Lunch and Learn Series: Trends in European Clinical Trials

Are you considering conducting a medical device trial in Europe? Join us for an infromation lunch and learn to discuss the Trends in European Clinical Trials.

This session focuses on current and best practices in conducting global trials to obtain various regulatory approvals including:

• Literature review vs. prospective data needs for CE Marking
• Pros and cons of using EU to support US approval
• EU site seletion considerations: country requirements and timelines
• Considerations for post-market trials
• Registries vs. Trials
• Vigilance and safety reporting