Newsletter | October 22, 2024

10.22.24 -- AI's Potential Must Reconcile With R&D And Regulatory Bottlenecks

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Webinar: 5 Strategies to Dramatically Improve Clinical Data Quality

Join us on October 29th as we unravel the complexities of fragmented data systems, emphasizing the urgent need to adopt technology and processes that harmonize diverse data sources and ensure quality throughout the clinical trial data lifecycle. Discover how to unify data management and augment processes with automation and AI to find and fix data quality issues sooner and more efficiently. Click here to learn more.

CLINICAL TRIAL TECHNOLOGY

AI's Potential Must Reconcile With R&D And Regulatory Bottlenecks

Guest Column | By Daniel Chancellor, Evaluate

Evaluate's Daniel Chancellor explains that by working together to expand AI resources and adapt regulatory frameworks, the FDA and others can ensure the benefits of AI are fully realized while maintaining high standards of safety and efficacy.

Why You Should Expect More from Your IRT/RTSM

e-book | Perceptive Inc

Explore the need for advanced capabilities beyond basic RTSM, and the importance of having experienced teams behind IRT solutions to navigate complexities and ensure successful trial execution.

Medable Platform Delivers >90% eCOA Adherence And Scalability

Case Study | Medable

Discover how eCOA use drove >90% adherence across an extensive weight management master protocol clinical trial with multiple sub-studies across 70+ research sites.

Reduced Sample Sizes And Shorter Durations With Digital Biomarkers

Case Study | Roche Information Solutions

Digital biomarkers provide a pathway to the future where clinical trial sponsors can potentially benefit from reduced trial duration and sample size. Learn more about these benefits from a simulated study.

Deploy eConsent Around The World With Confidence

Video | IQVIA Technologies

Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.

Is It Worth The Effort To Switch To Veeva's EDC?

Video | Veeva Systems, Inc.

Kronos Bio discusses how their oncology biotech switched to Vault EDC for faster, more flexible builds.

The Diversity Imperative: EDC And Inclusive Clinical Trials

Video | Anju Software

In this EDC Showcase, experts delve into the crucial role of EDC in fostering diversity within clinical trials. Discover adaptable solutions for a more inclusive and efficient clinical workflow.

eCOA / ePRO

Product | Medrio

Enable convenient and accurate outcome reporting, enhancing data quality and study efficiency with electronic patient-reported outcomes (ePRO) and electronic clinical outcome assessments (eCOA).

eISF In European Clinical Trials And How eBinders Can Help

Article | Florence Healthcare

By addressing the unique hurdles tied to regulations in European clinical trials, eBinders offer a streamlined approach to managing electronic trial documentation.

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With ICH M11 expected to be adopted by the end of the year, the next Clinical Leader Live digital event will host a panel discussion on the advantages of improving and simplifying the dataflow of clinical trials but also the challenges associated with creating a connected digital dataflow, including digital health channels, that spans from protocol to data collection to CSR. Register today and join us on 10/31 at 1 pm ET (10 am PT).

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  • 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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