Insights On Clinical Technologies
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Digital Endpoint Resource Guide: Dermatology
11/20/2023
Dive into recommendations released by the FDA regarding the use of DHTs in clinical development and the opportunities wearable-based digital endpoints present to the life sciences industry.
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Maximizing Site Performance: The Hidden Benefits Of Unified eConsent And EDC
12/6/2024
Disconnected systems for eConsent and EDC create inefficiencies that burden clinical trial teams, but modern integrated platform solutions are streamlining operations.
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Generate Accurate And Meaningful Insights With AI
6/25/2025
Find out how you can curate unstructured healthcare data in a validated manner, unlocking key patient insights across the drug development lifecycle.
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Modern Post-Market Trials Driven By RWD – Is Your EDC Ready?
7/7/2025
Explore the transformative role of real-world data (RWD) and advanced Electronic Data Capture (EDC) systems in post-market research, marking a departure from traditional Phase IV trials.
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Navigating Regulatory And Privacy Updates In Clinical Trials
3/21/2025
Explore how the guide for eRegulatory adoption in Canada provides resources to help stakeholders navigate these changes and enhance participant engagement and retention in clinical trials.
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Risk-Mitigation Recommendations When Using Technology
9/12/2023
Recent FDA and EMA guidance highlight the importance of human involvement when using technology in clinical trials.
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How Digital Innovation Can Inform RWE-Led Decision-Making
1/17/2025
Real-world evidence (RWE) is changing how healthcare products are developed and marketed. Learn how digital innovations are helping companies leverage RWE to make better decisions.
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Accelerate Respiratory Disease Trials: A Guide To Digital Endpoints
4/15/2025
Learn how wearables and DHTs are alleviating the trial participation burden, increasing the likelihood of trial success, and enhancing the overall management of these conditions.
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eConsent Readiness In 24 Countries
3/12/2024
Discover how regulatory bodies worldwide, including the U.S. Food and Drug Administration and the European Medicines Agency, are now championing the shift towards eConsent adoption.
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eSource vs. EDC: Reimagining Your Clinical Trials
5/29/2025
Explore how an eSource approach to clinical trial data can reduce site burden, eliminate double data entry, minimize queries, and enhance remote monitoring.