Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Automate core regulatory report documents across the CTD pyramid and dramatically accelerate submission timelines.
Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Automate core regulatory report documents across the CTD pyramid and dramatically accelerate submission timelines.
Event
Medical writers are the last step in the clinical process before getting a drug to market. As a result, they are often faced with tightening deadlines and pressure from internal stakeholders. So, where does technology fit into their writing process?
AI tools can eliminate potential delays before they happen and automate tedious data interpretation processes. In this webinar, panelists from Yseop and Docuvera will discuss disruption in the drug documentation approval process and how innovative technology is increasing productivity for authors, reducing the cost per document, and delivering faster time to submission. They will discuss:
Date: March 24, 2022
Time: 11am EDT
Panelists: Janet Schorr from Docuvera & Emmanuel Walckenaer from Yseop
With the participation of:
Let’s start automating your data to narratives today!