Appointment Announcement – Jamie Moss, Executive Chair

We’re excited to announce the appointment of Jamie Moss, new Executive Chair.

The Quality Issue – August 2025

Join our ICH E6(R3) live panel webinar, explore ACRO highlights, and connect with TRI this autumn.

The Quality Issue – July 2025

ICH E6(R3) is now effective in the EU, marking a pivotal shift in clinical trial oversight. This issue breaks down what it means and how to stay ahead.

TRI launches major overhaul of OPRA-CM

TRI’s reimagined OPRA-CM platform delivers on the true promise of RBQM, cutting through complexity to enable smarter, faster, and more focused centralized monitoring.

The Quality Issue – May 2025

In this edition, we mark National Clinical Trials Day, spotlight new Tufts CSDD research on monitoring trends, and share must-attend events.

The Quality Issue – April 2025

From Vancouver to London, this edition highlights must-attend RBQM events that offer fresh insights, regulatory updates, and real-world strategies to elevate your clinical trial oversight.

SCDM – April 2025

We’re heading to Brussels for SCDM 2025 EMEA! Visit TRI at Booth 21 to discover how our reimagined OPRA-CM platform is transforming centralized monitoring and driving RBQM success.

The Quality Issue – February 2025

In this edition, we reflect on two standout events, RBQM Summit and SCOPE 2025.

The Quality Issue – January 2025

We spotlight major developments in clinical research, from new FDA biopsy guidance and the EU’s CTIS transition deadline.

TRI Joins Veeva’s Product Partner Program

TRI has joined Veeva’s Product Partner Program, integrating OPRA with Vault EDC to deliver faster, smarter RBQM.