Registration is complimentary and required to attend.
About this webinar:
Clinical research site staff are facing an overwhelming amount of data collection per study, and inefficiencies in transferring that data from electronic health records (EHRs) into electronic data capture (EDC) systems compounds that burden. Ultimately, that results in compromised data quality and delays in reporting.
This webinar will cover how automated EHR-to-EDC technology reduces the data management burden for sites and sponsors and enhances overall efficiency in clinical trials. This approach enables researchers to save time and money, hit study milestones faster, and advance research for patients sooner.
Following a research study of three Academic Medical Centers across four industry-sponsored Phase I clinical trials, this webinar will showcase the efficiency benefits of a fit-for-purpose tool in:
- Enhancing the transfer of study data from the EHR into the EDC
- Reducing data queries
- Accelerating data-cleaning timelines
After the research presentation, you’ll have the opportunity to participate in a live Q&A with the speakers, going deeper into the practical applications, future adoption, and change management around EHR-to-EDC technology.
Attendees will walk away understanding:
- Tangible examples of how EHR-to-EDC technology is increasing the efficiency of trial data acquisition and management and lowering the burden to site staff
- Change management strategies required for successful implementation
This webinar is intended for the pharma R&D industry:
Presenters:
- Ivy Altomare, MD, Senior Medical Director, Flatiron Health
- Addie Shelley, Product Manager, Flatiron Health
- Paul Salcuni, MPH, Senior Data Scientist
About Flatiron Health:
About DPHARM, the webinar’s associated conference:
Registration is complimentary and required to attend.
