The Data Lifecycle: Leveraging Best Practices and Institutional Requirements for High-Quality Data and Reporting

Event Details

Purpose

This is the third webinar in a three-part series titled, “Strategic research project planning, data collection, and data management.”

Speakers

Patti Young
Regulatory Affairs Specialist
Clinical Operations, Office of the Clinical Director
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Courtney Duncan, M.S.W., L.C.S.W.
QA/QI Lead
Office of the Clinical Director
NIDDK

Marika Heinicke, Pharm.D., BCGP
Regulatory Affairs Specialist
Office of Clinical Research Support
NIDDK

Veronica Sansing-Foster, Ph.D.
Regulatory Affairs Specialist
Office of Clinical Research Support
NIDDK

Emma J. Stinson, M.P.H.
Biostatistician
Phoenix Epidemiology & Clinical Research Branch
NIDDK

Learning Objectives

1. To understand best practices for research safety monitoring and reporting.
2. To reflect on the importance of ongoing data review to ensure data integrity.
3. To review successful strategies for timely reporting of clinical data in CT.gov for regulatory compliance.

Agenda