Newsletter | August 26, 2026

08.26.26 -- Explore AI-Driven Data Insights And Tools Reshaping Research

The AI Paradox In Clinical Trials

Video | TruTechnologies

AI is advancing the way clinical trial results are analyzed and interpreted. But those advancements still depend on the quality and reliability of the data generated during the trial itself.

Clinical Research Without Borders

Webinar | Scout

Understanding the global clinical trial landscape is crucial in our interconnected world, as these trials are pivotal for advancing medical innovation. Explore strategies for navigating these global studies.

Leveraging Functional Service Providers For Drug Development Efficiency

Webinar | Worldwide Flex

Discover how functional service providers (FSPs) are reshaping clinical research by offering specialized expertise, flexible resources, and cost-effective solutions.

cGMP Compliant Pharmacy

Video | Dr. Vince Clinical Research

See how experienced compounding support helps ensure study drugs are prepared accurately and consistently across administration routes, meeting cGMP requirements while supporting clinical protocols.

RTSM Red Flags: When It's Time To Switch IRT/RTSM Software

Video | Korio

This clip outlines the key warning signs that an RTSM is no longer meeting study needs and offers practical guidance for recognizing risk early and making decisions that support trial continuity.

From Data Overload to Trial Insight With AI

Video | PPD Clinical Research Business of Thermo Fisher Scientific

AI-enabled clinical trial technology enables faster processing of large data volumes, thereby enhancing workflows, easing the burden on busy trial teams, and protecting patients.

Overview Of Central eSource Platform

Video | CRIO

Central eSource improves trial outcomes and transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework.

Trial Design Choices Determine Who Gets Access

Video | Clinical Leader

When asked what advice they have for sponsors, sites, or regulators, Natalie Monegro talks about the issues we can control from the onset of the trial that affect inclusiveness.

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