June 22nd 2023
Study Health Check provides early identification of issues related to protocol deviations and determines objective measures of site-specific versus study-wide performance.
September 22nd 2022
Clinical trials must rely on internet surveys to incorporate the needs of industry and patients, but how can results be improved?
September 7th 2022
How optimizing RBQM risk detection reduces the efforts caused by false signals.
August 3rd 2022
Survey among readers evaluates the trajectory of RWD and how it can be more widely adopted.
April 22nd 2022
Digital twins, defined as a typical demographic patient profile in a specific population, have the potential to help clinical trial design.
Strategic Immunogenicity Testing
Overcoming method validation challenges for trial populations during biologic drug development.
ePRO vs. Paper
The financial advantages of using ePRO over paper-based diaries when conducting clinical trials.
EDC & EHR Integration
Lessons learned along the journey to merge electronic platforms in clinical research and health care.
The Upfront Cost Hurdle of EDC
Although costs can force some sponsors to think twice, data show downstream savings add up.
Data Integration in the Age of Global Trials
The difference a clinical trial management system can make in integrating a global workforce.
Increasing Study Sensitivity in Early Trials
How using eDiaries in Phase II can increase power while reducing subject size and costs.
Optimize Your Imaging
Delays and expenses can be spared by crafting plans earlier and more methodically
Reducing Risk Through Mitigation Strategies
Proactive risk management helps pharma protect their product development investments and future.
Rescuing an EDC Study
Three-phase approach to make a midstudy vendor transition less painful.
Improving Site Efficiency and Productivity
Real-life examples of how a clinical trial management system impacted work-life for the better at five sites.