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By Abby Proch, executive editor for guest columns, Clinical Leader | At the recent SCOPE Summit, four experts in data management, monitoring, site operations, and tech weighed the pros and cons of adopting bring-your-own-device (BYOD) requirements for clinical trial eCOAs. | |
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| Overcoming Issues Of Non-Enrolling Sites In Clinical Trials | White Paper | By Dave Hiltbrand and Dave Berry, Thermo Fisher Scientific | Explore the challenges of non-enrolling sites in clinical trials, focusing on the benefits of leveraging artificial intelligence (AI) and machine learning (ML) in addressing those issues. |
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| 3 IRT Tactics Being Used To Streamline Supply Logistics | Article | By Maxime Schuchewytsch, IQVIA Technologies | Shipping and storing leading-edge therapeutics require complex logistics, but enhanced automation and process simplification ensure that sites and patients have the drugs they need when they need them. |
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| A Data-Driven Approach To Clinical Trial Site Selection | Article | By Martina Micaletto, Alan Kott, and Petra Reksoprodjo, Signant Health | By incorporating data-driven site selection and verification, sponsors can optimize resource allocation, enhance protocol compliance, and improve overall trial integrity. |
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| Transforming Field Rep Success | Article | By Steven Anzuini, Anju Software | As the demand for efficient medical information access increases, adopting information management tools is essential. |
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