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2025 DIA Annual Meeting: Why AI and Automation Are Set to Become the New Normal in Clinical Research
Peter Ronco, CEO, Emmes, shares his long-term vision for artificial intelligence in clinical research, from making automation ...
Using a recent survey on the adoption of AI/ML conducted by the Tufts CSDD as context, pharma leaders discussed how they are ...
Peter Ronco, CEO, Emmes, explains how the company is investing in transparent goal setting, comprehensive education, and ...
In an interview with ACT senior editor Andy Studna at the 2025 DIA Global Annual Meeting, Carie Pierce, SVP, global head of ...
Cashin, MD, chief medical officer, Novotech, shares why clear communication, strong leadership, and cultural alignment are essential to building effective partnerships between CROs, sponsors, and ...
As wearable ECG technology advances, cardiac safety studies in clinical trials are evolving to capture richer, continuous ...
In this Q&A, Megan Bailey, EVP and president of central laboratories and international, Labcorp, discusses how central labs ...
In our June issue, explore how clinical research is adapting to regulatory changes, AI advancements, and modernizing trial ...
Navigating a complex drug development landscape, sponsors must rethink their approach to risk in study design and execution.
Cross-sector partnership launches EQBMED. Initially funded by PhRMA and established as a cross-sector collaborative, ...
Balancing the emerging benefits of AI in pharmacovigilance with new responsibilities and demands from regulators in enhancing ...
In this video interview, Matt Robinson, PhD, senior director, oncology research program, National Comprehensive Cancer ...
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