Webinar: Learn How to Reuse Patient Trial Data to Mitigate Go/No-Go Product Development Decision Risks

02/28/2018

Join us on Weds., Feb 28 at 12PM EST, for a complimentary webinar, “Learn How to Reuse Patient Trial Data to Mitigate Go/No-Go Product Development Decision Risks.”

Hear from Board Certified Oncologist and former SVP of Global Oncology at Merck KGaA, Reinhard Von Roemeling, who will draw on his extensive history in Oncology Therapy Research and share perspective on the industry's opportunities & challenges for better scientific validity, reducing the number of failed trials started, leveraging historical clinical trial data to enhance understanding of various diseases, and more!

You’ll also hear former FDA Deputy Director and current Medidata Director of Data Science, Ruthie Davi, PhD, explore the value of our Synthetic Control Data and 2017 Scrip Award-winning Synthetic Control Arms, which leverage our MEDS (Medidata Enterprise Data Store) clinical data repository to enable greater safety, efficacy and subgroup analyses in single arm trials -- further empowering you to make ‘go/no-go’ product development decisions after early-phase trials. 

Register Today!