Customize CTMS Dashboards for Every User

July 16, 2026

Customize CTMS Dashboards for Every User

Every clinical trial role requires different information. CRAs need to track upcoming monitoring visits, Project Managers need study performance metrics, and clinical operations teams need enrollment and site activity data.

In this video, see how Flex Databases CTMS allows every user to create a personalized dashboard without affecting other users. Learn how to add or remove report widgets, monitor real-time study metrics, and filter data by project, site, country, and other parameters. Personalized dashboards help teams quickly access the information they need to manage multiple clinical trials more efficiently.

Blog

July 17, 2026
Why Long-Established eClinical Platforms Are Slowing Down Modern Clinical Trials 

What Sponsors Should Really Look For When Choosing an eClinical Platform?  Today, every established vendor offers all kinds of system modules, document management capabilities, and a long list of compliance certifications.  On paper, they appear remarkably similar, making it increasingly difficult for sponsors and CROs to distinguish between solutions based on feature lists alone.  In reality, they couldn’t be more different.  Most enterprise eClinical platforms can […]

July 16, 2026
Customize CTMS Dashboards for Every User

Every clinical trial role requires different information. CRAs need to track upcoming monitoring visits, Project Managers need study performance metrics, and clinical operations teams need enrollment and site activity data. In this video, see how Flex Databases CTMS allows every user to create a personalized dashboard without affecting other users. Learn how to add or […]

July 15, 2026
How ITS Cut Manual Safety Tracking by 60% and Strengthened PV Oversight Across Clinical Trials

About Integrated Therapeutic Solutions Integrated Therapeutic Solutions (ITS) is a clinical research organization conducting multi-country clinical trials and supporting post-marketing needs across a growing sponsor portfolio. As case volumes increased, so did the complexity of managing pharmacovigilance activities from safety event intake and workflow tracking to regulatory reporting and cross-functional coordination with clinical operations teams. […]

July 7, 2026
Is Your EDC Really Modern If Someone Still Has to Re-Enter Every Serious Adverse Event?

Clinical industry has finally embraced AI, sponsors run decentralized trials and data is now collected in real time. But still one of the most critical workflows in every study – handling adverse events (AEs) – surprisingly depends on copy-paste. Most sponsors assume that if they have an Electronic Data Capture (EDC) system and a Pharmacovigilance […]

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