Newsletter | February 20, 2026

02.20.26 -- Sponsors Collect Too Much "Non-Essential" Data, Say Tufts And TransCelerate

CLINICAL DATA MANAGEMENT & ANALYTICS

Sponsors Collect Too Much "Non-Essential" Data, Say Tufts And TransCelerate

A collaboration between Tufts CSDD, Tufts School of Medicine, and TransCelereate BioPharma revealed just how much extra data sponsors are collecting — and why that's a problem.

The Connected Patient In Clinical Trials

Discover how digital innovation and patient-centric technologies are reshaping clinical trials by improving access, efficiency, and data-driven insights.

Empower Your Trial With Data And Evidence

Fuel your clinical development and decision-making with insights from fit-for-purpose data and evidence.

A New, AI-Augmented Horizon For Safety And Pharmacovigilance

Is your organization leveraging AI to maximize efficiency in safety and regulatory workflows? If not, explore how these technologies are slated to improve industry approaches in 2026.

Changing The Clinical Feasibility Game With AI

AI is only as good as the data it’s built upon. Our customized AI platforms are constructed on a foundation of trustworthy, carefully curated data to produce detailed, expert-driven responses.

The Big Impact Of Medable AI

Streamline your clinical trial study creation by automating and accelerating the eCOA build process. Generative AI models perform your repetitive configurations and significantly shorten build times.

Measuring A Wide Range Of CNS Effects In A Pharmacological Context

With nearly three decades of successful application, NeuroCart remains a gold standard in CNS pharmacology, supporting precise, data-driven decisions in drug development.

EHR To EDC Connectivity With TrialKit

Clinical sites use many different EHR and EMR systems, each with unique data structures. Explore flexible EHR to EDC solutions that allow teams to use this data without complex service engagements.

TRIAL MONITORING

How To Meet FDA Expectations For Hybrid And Decentralized Trial Oversight

Former FDA attorney Claire Davies shares strategies for meeting regulators' expectations for hybrid and decentralized clinical trial oversight.

Reducing Risk With Shift Left Testing

In today’s development landscape, where speed and resilience must go hand in hand, adopting a "Shift Left" mindset transforms testing from a bottleneck into a catalyst for innovation.

Yes, Your Study Is At Risk: Risk Mitigation Plans For Endpoints

Ocular endpoints often introduce unique bottlenecks that can stall enrollment and compromise data integrity. This presentation provides the tools for a streamlined, resilient clinical trial strategy.

CHOOSE YOUR OWN ADVENTURE

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)

Learn more about our personalized newsletters here.

Connect With Clinical Leader: