Newsletter | June 6, 2025

06.06.25 -- Medtech CEO Shares Lessons From FIH Implantable Glucose Monitor Trial

CLINICAL DATA MANAGEMENT & ANALYTICS

Feasibility/Site Selection Process Ripe For Improvement

One key to a more effective feasibility process is more transparent communications and collaboration between sponsors, CROs, and sites. Sponsors must provide clear information to each site to enable a more accurate recruitment assessment, and sites must properly digest the information to give an accurate projection. But how?

6 Ways Lab Data Can Improve Clinical Trials

Explore six key ways laboratory data strengthens the clinical trial process, focusing on how RWD enhances patient recruitment, accelerates screening workflows, and improves overall study outcomes.

What Is Electronic Data Capture And How Does It Simplify Data Management?

As EDC systems continue to evolve, they streamline workflows, enhance data security, and improve patient outcomes.

Harnessing AI: Drug Discovery And Early Disease Detection

The power of data and algorithms is unlocking new frontiers in healthcare. Pharma 2025 discussions focused on AI's role in revolutionizing drug discovery and early detection.

Quality Data From Verana Health For HEOR And Medical Affairs

Obtain real-world data on patient demographics, treatment patterns, and outcomes to help inform your future business decisions.

Data Monitoring Committee (DMC) Services

Let us build and manage your data monitoring committee or data safety monitoring board, ensuring oversight and the highest standards of data integrity and participant safety throughout your study.

Regulated Document Review

Enables secure real-time document review, co-authoring, and redaction in order to shorten the document review process by up to 65%.

TRIAL MONITORING

Medtech CEO Shares Lessons From FIH Implantable Glucose Monitor Trial

CEO and President Paul Goode, Ph.D., explores the implantable CBGM’s trial design, as well as the company’s approach to patient input, site selection, and more for its first-in-human trial.

The Future Of Remote Patient Monitoring In Decentralized Clinical Trials

Remote Patient Monitoring (RPM) is not just an innovation—it's a catalyst redefining how clinical research is conducted in the digital age.

Automated Trial Monitoring Workflows Make Small Teams More Efficient

A pharmaceutical therapy developer was looking to automate reports, confirmation letters, and follow-up letters. See what happened when they adopted a cloud-based solution for end-to-end trial management.

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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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