Newsletter | June 10, 2025

06.10.25 -- 7 Steps For Clinical Investigators To Implement A Robust AI Governance System

CLINICAL TRIAL TECHNOLOGY

7 Steps For Clinical Investigators To Implement A Robust AI Governance System

In part two of this series, Husch Blackwell LLP experts provide practical guidance for clinical investigators on overseeing the use of AI in clinical trials.

The Flexibility Of Reconsent In Clinical Trials

Explore the common misconceptions surrounding reconsent, as well as the reality of its ability to be a flexible, ethics-driven communication practice grounded in respect for participant autonomy.

Patient-Reported Outcome In Oncology Clinical Trials

As cancer therapies grow more complex and personalized, patient-reported outcomes (PROs) have emerged as a vital component of oncology research and care.

Parkinson's Disease: Leveraging Wearable DHTs

Wearable DHTs offer a solution to the challenges of measuring Parkinson's disease in clinical trials. Discover how these technologies can improve outcome measures and accelerate drug development.

eCOA Licensing Guide

In this comprehensive guide, IQVIA's eCOA library and licensing specialists, Kayla Doyle and Piero Bindi, explore five essential steps for obtaining licenses for the assessments required in your clinical trial.

Medidata CTMS Leads The Industry

The 2024 Everest Group PEAK Matrix assessment has named Medidata CTMS the leading Clinical Trial Management System (CTMS).

Central eSource: How Sponsors Can Leverage Site Technology

In this presentation, CRIO founder and co-CEO Raymond Nomizu delves into how sponsors can leverage the electronic source trend among sites through the use of Central eSource.

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  • Outsourcing Models | Regulatory & Compliance (Thursday)
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