WEBINAR: How to automate clinical data management
In pharmacovigilance, post market surveillance and many other areas of drug development, highly skilled team members spend an enormous amount of time systematically mapping out publications. This includes going through clinical trial reports and real world evidence, and extracting key data points such as adverse effects.
In this webinar, we covered how to:
👉 Automatically filter based on entities of interest and specific context.
👉 Extract data such as adverse effects, treatment and patient baseline characteristics.
👉 Save days of manual review time.