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| A 2025 Tufts CSDD–CRIO survey of 209 global investigative sites examined how clinical trial protocols are translated into practical source documents and tools. The research highlights inconsistent terminology, fragmented workflows, and inefficiencies in site-level source preparation. This webinar reviews key findings and identifies opportunities to improve efficiency and quality through better protocol driven source preparation. Click here to learn more. |
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CLINICAL TRIAL TECHNOLOGY |
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| Start With The Question, Not The Technology | Video | Clinical Leader Live | As a former FDA employee, Donna Rivera emphasizes defining the problem and regulatory context first to ensure any AI solution is fit for purpose. |
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| Enable Value-Based Evaluation Of Medicines | Product | CHDR | Trial home, CHDR’s dedicated strategy for off-site clinical trials, enables investigators to collect information as trial participants go about their day to day activities. |
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| A Modern Clinical Research Platform | Brochure | Castor | Explore a platform supporting secure integration of real-world data (RWD) from EHRs and tokenization, enabling rich, longitudinal insights, and flexible study designs. |
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| Central eSource: Leveraging Site Technology | Video | CRIO | In this presentation, CRIO founder and co-CEO Raymond Nomizu delves into how sponsors can leverage the electronic source trend among sites through the use of Central eSource. |
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CHOOSE YOUR OWN ADVENTURE |
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| You're receiving the Tuesday edition of the Clinical Leader newsletter, focusing on Clinical Trial Technology. To make changes to your newsletter selections, update your topic preferences. - Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
- Clinical Trial Technology (Tuesday)
- Decentralized Trials | Trial Management (Wednesday)
- Outsourcing Models | Regulatory & Compliance (Thursday)
- Clinical Data Management & Analytics | Trial Monitoring (Friday)
Learn more about our personalized newsletters here. |
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