Date: Tuesday, October 19th, 2021
Time: 08:00am PT / 11:00am ET / 5:00pm CEST
A growing number of our Sponsor clients monitor or plan to monitor certain ongoing studies using interim data loads as and when they become available from CROs and specialty labs.
Hear directly from senior industry partners as we host a discussion on how analysis-ready data, in short, leads to submission-ready data.
This discussion will be co-hosted by:
- Dragomir Ivanov Draganov, MD, PhD, Data Science Lead (Pharmaceutical Sciences) at Roche
- Dessi McEntee, Nonclinical Safety Study Manager & Operations Lead at Epizyme
- Laura Kaufman, PhD, Senior Toxicologist and Independent Consultant and Board Certified Toxicologist.
We invite you to submit questions in advance (without attribution) by e-mailing firstname.lastname@example.org.
To register for the webinar, please fill in the form on the right.