Newsletter | September 19, 2023

09.19.23 -- Navigating The Hype Of AI

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Free scientific video series: Signant’s Clinical Viewpoints

At Signant Health, we combine our technology with robust clinical, scientific, and regulatory expertise to guide your study from design to regulatory submission. In this video series, Chief Medical Officer Dawie Wessels leads discussions with a selection of our in-house clinicians, scientists, medical practitioners, and key opinion leaders about how they ensure the best practices and solutions are in place to help clinical research programs succeed.

CLINICAL TRIAL TECHNOLOGY

Navigating The Hype Of AI In Clinical Research

Guest Column | By Sarah Valentine, Digital Medicine Society (DiMe)

When you consider the rising cost of healthcare in America, a shortage amounting to tens of thousands of physicians, and economic headwinds stirring fear across the field, we can’t afford to not use AI. We shouldn’t be asking ourselves questions of why, but rather, why not. But that begs a new question: Why haven’t we seen the impact, adoption, and value of AI more broadly across clinical research?

Advancing Clinical Research With Modern Technology

Article | By Laura McWhinney, ISR Reports

Explore innovative technologies used in clinical trials and the challenges teams often face during adoption in this Decentralized Clinical Trials Market Outlook report.

Focusing On Patient-Reported Outcome Measures And eConsent

Article | Medable

Learn how digital solutions can contribute to a more participant-centered approach and potentially enhance the regulatory utility of PRO data while improving the overall quality and efficiency.

Essity Uses eConsent To Optimize Enrollment

Case Study | Castor

See how a global hygiene and health company was able to deploy virtual methods through a strategic partnership to recruit and retain participants, streamline consent, and analyze patient data.

eTMF As A Factory: Key eTMF Elements And Practices For High-Volume, High-Quality Processing

White Paper | By Kathie Clark, IQVIA Technologies

In an ideal scenario, the eTMF would operate like a well-oiled factory. Examine some of the key factors that would support making “the eTMF factory” a reality.

Accelerate Study Start-Up With Flexible EDC Technology

Brochure | Mednet

Enable researchers to quickly and accurately collect patient data in real-time and eliminate the need for paper-based data collection methods, saving time and reducing the risk of errors.

IQVIA’s Integrated IRT eCOA Platform

Datasheet | IQVIA Technologies

Improve study quality, accelerate decision making, and reduce site and sponsor burden by using IQVIA’s integrated interactive response technology and electronic clinical outcome assessment solution.

Experience The YPrime Difference

Video | YPrime

At YPrime, our teams help to create positive impacts by bringing life-changing therapies to market.

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