Webinar attendees will:

• Review regulatory requirements and challenges for long-term follow-up
• Hear a discussion on current pragmatic approaches in the trial population and real world data sources in the post-approval process
• Explore future ideas for long-term follow-up including tokenization, EMR to EDC, and others

If you are based in Americas or EMEA, please CLICK HERE to register.

If you are based in Asia-Pacific or Japan, please CLICK HERE to register.