Newsletter | January 14, 2025

01.14.25 -- How AI Will Transform Health Equity In Clinical Trials In 2025

SPONSOR

Webinar: Can We Enable Clinical Trial Operations Without Human-In-The-Loop?

To drive forward the promising pipeline of breakthrough therapies while curbing costs, industry futurists are putting their bets on technological advancements and GenAI to reshape the drug development life cycle. This session is an invitation to rethink traditional approaches, consider innovative risk mitigation strategies, and envision a future where clinical trials are faster and more efficient but also potentially free from human limitations. Register here.

CLINICAL TRIAL TECHNOLOGY

How AI Will Transform Health Equity In Clinical Trials In 2025

Click Therapeutics' CMO/CSO Shaheen Lakhan, MD, Ph.D., FAAN explains how the shift toward AI is the first step in addressing diversity in clinical trials.

Solutions For Sponsors Utilizing Drafted Guidance For PROs

Explore the challenges pharmaceutical companies face in implementing PROs in cancer clinical trials as outlined in the FDA’s draft guidance, as well as strategies to overcome these obstacles.

Unleash The Power Of IQVIA Complete Consent

In this presentation, Vinita Navadgi and Amy Koller from IQVIA Complete Consent provide an in-depth exploration of the eConsent landscape.

The Difference Between A Traditional IRT And Rave RTSM

Examine the differences between Traditional IRT and Rave RTSM, highlighting key attributes like workflow integration, user management, and overall impact on clinical trial operations.

The Hidden Benefits Of Unified eConsent And EDC For Sites

Disconnected systems for eConsent and EDC create inefficiencies that burden clinical trial teams, but modern integrated platform solutions are streamlining operations.

Flexible Integrations To Reduce Risks And Increase Efficiencies

Learn how a trial team kept the blind of central lab samples and patient treatment across a Phase III and extension trial, whilst optimizing the supply chain.

Deliver A Complex eConsent Experience

Drive compliance and retention throughout your trial and keep your patients informed using a system that's easy to configure and manage from site to subject.

Bridging The Gap Between Research & Healthcare

This platform offers precision source data capture, including secure EHR data retrieval to auto-populate trial eCRFs, a seamless user experience with single sign-on, and real-time data visualization.

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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)

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