Newsletter | January 10, 2025

01.10.25 -- Lab Manual Gaps: Sabotaging Data One Sample At A Time

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Webinar: Step Inside IQVIA One Home for Sites™

Clinical research sites have been asking for single sign-on (SSO) for a decade. In this webinar, you’ll learn why 2025 will be the year when sites will finally begin to feel relief from technology overload. Discover why whether you’re with a sponsor, site, and technology vendor, it's time for you to move into One Home and join this industry collaboration. Click here to learn more.

TRIAL MONITORING

A Data-Driven Approach That Could Change Mental Healthcare In 2025… And Beyond

Guest Column | By Greg Hajcak, Ph.D., Universal Brain

Heterogeneity of patient populations combined with subjective clinical interpretation often results in imprecise treatments, frustrated patients, and poor outcomes, says Greg Hajcak, Ph.D. Here, he argues for a data-driven approach, also called “precision psychiatry,” to personalize clinical trials and care.

U.S. Clinical Labels 101: Steps To Ensure Accuracy

Article | Ropack Pharma Solutions

Determining a drug candidate’s probability of commercial success is a significant phase in the drug development process. There is no room for error.

The Key To Compliance, Patient Safety, And Risk Based Monitoring

Datasheet | IQVIA Technologies

eClinical technologies are becoming more commonplace in drug development. Uncover how digital solutions are helping sponsors improve efficiency and accuracy within their clinical trials.

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AI is transforming clinical trials — are you ready to harness its potential? Join Clinical Leader Live on January 14th to explore real-world applications of AI that optimize trial design, enhance data analysis, and accelerate timelines. Don’t miss this chance to stay ahead in clinical research! Attendance is free thanks to the support of The PPD clinical research business of Thermo Fisher Scientific.

CLINICAL DATA MANAGEMENT & ANALYTICS

Lab Manual Gaps: Sabotaging Data One Sample At A Time

Guest Column | By Elena Sinclair, FlexPoint Bio

In part two of this series on lab manuals, FlexPoint Bio Founder and CEO Elena Sinclair discusses the criticality of sample and process quality.

Dear Clinical Data Reviewer, Listing Reviews Don't Have to Be Painful.

Article | ThoughtSphere

Struggling with cumbersome listing reviews? Discover how modern SaaS tech and collaborative workflows streamline data consistency for Medical Monitors and Data Managers.

Digging Through The Hype: Can AI/ML Assist Clinical Development?

Webinar | Revvity Signals Software, Inc.

AI has great potential to enhance the efforts of your team members by accelerating data interactions. Watch this webinar and discover how AI can improve clinical trial outcomes and data management.

Defining 'Evidence Generation' Within Modern Clinical Trials

Article | By Colin Weller, Medable

Learn how this distinctive approach centered on enabling clinical trial sponsors to gather data and generate evidence ensures the successful acquisition of diverse information.

Clinical Intelligence For CROs

Datasheet | Anju Software

Discover how TA Scan, a business intelligence solution, combines and connects global trial, presentation, and publication data to improve RFP support, bid defenses, and operationalization.

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You're receiving the Friday edition of the Clinical Leader newsletter, focusing on Clinical Data Management & Analytics and Trial Monitoring. 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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