eSource by the numbers
- 20% of study costs go to data duplication and verification.
- Manual entry costs up to $50K per patient; eSource cuts burden by 50%.
- AI-driven eSource reduces errors by 99% and standardizes data.
- Interoperability and compliance remain key adoption barriers.
- Phase I trials to be fully eSource-enabled within two years.
Advarra and IgniteData have announced a new partnership, enabling secure clinical data transfer between research sites’ instances of Advarra's eSource and electronic data capture (EDC) solutions, electronic health record (EHR) systems, and sponsor EDC systems.1
Enabling data collection for commercial sites
For commercial sites without an EHR system, this new partnership will enable data collection in Advarra's eSource platform to be transmitted through IgniteData's Archer connector into the sponsor's preferred EDC system.
In a company press release, Scott Uebele, chief operating officer at Advarra, said: "Sites have long struggled with fragmented, disconnected solutions that make data exchange cumbersome and error-prone. With 90 of the top 125 academic medical centers, 90% of NCI-Designated Cancer Centers, and over 300 enterprise research sites leveraging Advarra's site technology—including OnCore CTMS, Clinical Conductor CTMS, eReg, eSource, and EDC—we're dedicated to bringing innovations to market that simplify processes.”
Efficient data transfer for academic and cancer research centers
Meanwhile, for academic medical centers and cancer centers, the integration will allow for the transfer of data between the center’s EHR system through IgniteData's Archer platform into Advarra's EDC.
In the release, Zach Taft, CEO of IgniteData, added: "Unlike other vendor connectors that require organizations to use a single, proprietary platform to unlock efficiencies, our partnership with Advarra will give research sites the flexibility to use the tools they choose.”
Data collection challenges in oncology trials
Efficient data collection has long been a challenge for the clinical research industry, especially in oncology trials. A recent article published in Applied Clinical Trials on scaling eSource-enabled clinical trials highlighted opportunities to address this challenge from a hospital perspective. The authors found: