Articles, App Notes, Case Studies, & White Papers
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Empowering Oncology Research With The Right Technology Solutions
10/25/2023
Explore how advanced technology solutions have the potential to simplify the operational aspects of oncology trials.
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How Can Sponsors Enable Research-Naïve Clinical Trial Sites
8/8/2025
Clinical trial capacity in the U.S. is heavily concentrated, and technology is playing a critical role in enabling a shift to expanding site networks and alleviating the burden on sites and patients.
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Aligning Global Standards For ICH E6(R3) And Artificial Intelligence
12/11/2025
Global standards and AI are transforming clinical research. Learn why mastering ICH E6(R3) and risk-based compliance is critical for data integrity and future success.
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Key Insights From The FDA's DHT Guidance
3/12/2024
Check out a summary of the FDA’s guidance Framework for the Use of DHTs in Clinical Trials and what it means for sponsors and investigators using these innovative tools.
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How Real-Time eTMFs Are Helping Keep Trials On Track
3/2/2023
Learn how real-time dashboards assist with the sorting of information so clinical trial and medical affairs teams know what needs to be done, when, and by whom.
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Defining 'Evidence Generation' Within Modern Clinical Trials
1/26/2024
Learn how this distinctive approach centered on enabling clinical trial sponsors to gather data and generate evidence ensures the successful acquisition of diverse information.
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7 eCOA Design Recommendations: Insights From Sites And CRAs
2/20/2024
Signant joined a group of C-Path members including other eCOA solution providers, sponsors, and regulators for a GBTI project that revealed several opportunities to improve eCOA usability and flexibility.
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The Future Of Remote Patient Monitoring In Decentralized Clinical Trials
5/8/2025
Remote Patient Monitoring (RPM) is not just an innovation—it's a catalyst redefining how clinical research is conducted in the digital age.
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Paving The Way For Virtual Trials In Neurology: A Fully Remote ALS Study
5/23/2023
The COVID-19 pandemic has completely changed the way we think about clinical research and care. Clinical trials, a vital component of the drug development process, were heavily disrupted because patients, often with weakened immune systems, could not visit hospitals and research sites.
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A Data-Driven Approach To Clinical Trial Site Selection
3/24/2025
By incorporating data-driven site selection and verification, sponsors can optimize resource allocation, enhance protocol compliance, and improve overall trial integrity.