Archive: 2024
Bridging the Gap – TEFCA, Healthcare Data Interoperability, and Clinical Research Use Cases
Reading Time: 5 minutesAccessing data from multiple electronic health record (EHR) systems results in… Read More
Challenges & Opportunities in Implementing Generative AI
Reading Time: 2 minutesThe potential that generative AI may have on nearly all industries… Read More
The Essential 5 Es for Operationalizing AI in Clinical Data Management
Reading Time: 4 minutesModern clinical trials are accelerating towards increased complexity, with their expanding… Read More
An Introduction to Interoperability in Healthcare
Reading Time: 10 minutesWhat Is Interoperability in Healthcare? Healthcare interoperability is the… Read More
Shaping Tomorrow’s Trials: Takeaways from Medidata NEXT New York 2024
Reading Time: 3 minutesAs the clinical trial landscape evolves, so do the demands for… Read More
Medidata Presents Research at ASH 2024
Reading Time: 3 minutes Blood cancers make up a large portion of cancer types—these… Read More
The Role of Source Data Verification (SDV) and Source Data Review (SDR) in Driving Clinical Trial Data Quality
In a risk-based monitoring (RBM) update released in January, TransCelerate defined source data verification (SDV) as “the process by which data within the case report form (CRF) or other data collection systems are compared to the original source of information (and vice versa).” Read More
National Breast Cancer Awareness Month: Redefining Hope in HER-2 Low
Reading Time: 3 minutesBreast Cancer Awareness Month has occurred every October for over four… Read More
Diversity in Clinical Trials: FDA Draft Guidance on Diversity Action Plan Requirements
Reading Time: 3 minutesThis blog was authored by Ashni Parekh, Global Compliance… Read More
3 Ways to Approach Challenges During Study Feasibility Processes
Reading Time: 2 minutesIdentifying high performing sites for a clinical trial is a crucial… Read More
