Planning For and Addressing Missing Data in Mobile Clinical Trials

This podcast presents a session on planning for and addressing missing data form the 2019 Mobile in Clinical Trials conference. 

When a protocol dictates a set period of time for data collection, what happens when there's a gap in the data due to technical glitches or human error? What are the regulatory and operational implications? Discussion points include:

• How to prepare for missing data
• How do we handle missing data?
• How to rewrite protocols so that you avoid the trap
• Forewarning and communicating with regulators
• Regulatory advice on how to address missing data

Moderator:

Jennifer Goldsack, MBA, Executive Director, Digital Medicine Society (DiMe)

Panelists:

Ariel Dowling, PhD, Associate Director of Digital Clinical Devices, Data Sciences Institute, Takeda Pharmaceuticals

Marie McCarthy, MBA, Senior Director of Product Innovation, Information Technology, ICON plc

Carrie Northcott, PhD, Project Team Lead, Early Clinical Development, Digital Medicine, Pfizer

Shyamal Patel, PhD, Director of Data Science, Digital Medicine & Translational Imaging, Pfizer

The 2020 Mobile in Clinical Trials event will take place on September 21. Learn more here.