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February 7, 2025
At EUCROF 2025 in Copenhagen, Monique Dugueperoux, our Business Development Manager, attended a panel discussion on home trial services, where key stakeholders—sponsors, patients, sites, CROs, and health authorities—shared insights on the future of decentralized clinical trials (DCTs).
💡 Patients’ voices must remain central in decentralized clinical trials (DCTs).
The rise of decentralized trials has brought significant advancements in clinical research, from remote patient monitoring to digital tools that streamline data collection. But as technology continues to shape the future of trials, one critical question remains: Are we truly designing trials with patients in mind?
True innovation goes beyond digital solutions. Trials must be accessible, inclusive, and designed with patients in mind. The discussion at EUCROF 2025 reinforced the need to balance innovation, compliance, and real-world patient needs to ensure DCTs work for everyone.
As decentralized trials continue to evolve, keeping patient voices at the core will be essential. Meaningful change happens when all stakeholders—sponsors, sites, regulators, and, most importantly, patients—collaborate to shape the future of clinical research. How can the industry strike the right balance between innovation, compliance, and patient engagement? These discussions are just the beginning.
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Clincase EDC Implementation: Supporting Real-World Study Workflows
Clincase’s hybrid methodology brings structure and flexibility to every EDC implementation. In this article, our Implementation Manager, Caroline Chong, and her team walk through how that approach takes shape in real-world studies — from understanding complex protocols to delivering tailored system configurations.
How Clincase’s Hybrid Methodology Keeps EDC Implementation Agile, Focused, and On Track
Every successful clinical trial starts with a team that knows how to turn complex protocols into working systems. At Clincase, we use a hybrid project management methodology that blends structure and flexibility to guide EDC implementation from planning through go-live. In this article, developed with our Implementation Manager, Caroline Chong, we explain how her team supports sponsors and CROs by delivering setups that align with operational workflows and meet regulatory requirements.
Why Choosing the Right EDC System Is Critical for Clinical Trial Success
Clinical trials are growing more complex — not just scientifically, but operationally. As protocols evolve and timelines tighten, mid-sized CROs must deliver faster, more tailored trials with leaner teams. Choosing the right EDC system is critical to keeping pace and staying competitive.