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By Dan Schell, chief editor, Clinical Leader | It’s one thing to implement RBM (risk-based monitoring) components like central monitoring or initial risk assessments, but if you’re still doing 100% SDR/SDV, you’re not maximizing the benefits of this approach. So what’s the holdup? | |
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| A Strategic Framework For Positive Site-Sponsor Relationships | Article | By Matthew Jones and Julia Scanlon, IQVIA Technologies | Through an examination of evolving trial strategies and implementation, we aim to lay the groundwork for a collaborative, mutually beneficial atmosphere, ultimately leading to a sustainable competitive edge. |
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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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| How FAIR Data Principles Power Clinical Analytics Success | Webinar | Revvity Signals Software, Inc. | Explore key challenges in accessing and preparing analytics-ready clinical data, how FAIR guiding principles can help maximize the value of clinical trial data, and the impact of innovative analytics. |
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| Elevating Rater Training For More Reliable Study Outcomes | Article | By Marcela Roy, MA, Juliet Brown, Ph.D., Martina Micaletto, and Gary Sachs, MD, Signant Health | Well-trained raters are key to generating high-quality, consistent clinical trial data. Explore a program offering customized training tailored to the experience levels of raters. |
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