e-Learning

Advance Clinical Trial Expertise and Stay Compliant

Equip your clinical teams to deliver trials that meet the highest standards of quality and compliance. Our expert-led, scalable training, aligned with ICH E6(R3) and other evolving regulations, ensures your team stays ahead.

Good Clinical Practice

Take our CPD-Certified e-learning course on Good Clinical Practice to learn everything you need to know about;

Introduction to Good Clinical Practice
Applying ICH E6(R3) principles to real-world trial scenarios
Understand GCP principles in relation to your role
Key GCP responsibilities for IRB/IEC & Sponsors
The importance of RBQM in clinical trials

ICH E8 (R1)

Take our e-learning course to learn everything you need to know about;

Risk Assessment and Controls

Take our e-learning course to learn everything you need to know about;

Why TRI e-Learning?

Whether you’re onboarding new staff or reinforcing best practices, TRI e-Learning helps your team stay compliant and confident.

Focused on What Matters

Each module covers essential principles, aligned with ICH E6(R3). Host on your own LMS or use TRI's secure e-learning platform.

Confidence Through Interactivity

Animated, scenario-based learning keeps teams engaged , whilst interactive quizzes reinforce understanding.

Efficiency at Scale

Easy to roll out across global teams, saving time, effort and cost compared to traditional training, with an intuitive content. interface

Why Choose TRI?

Trusted

Dependable software. Genuine trust. TRI delivers, on time, at scale, with clarity.

Responsive

In a rigid industry, we’re the human touch: pragmatic, responsive, and known by name.

Innovative

We lead, not follow. TRI is fast-moving and data-informed, staying ahead of Sponsor and CRO needs.

TRI Insights & News

Why Low-Volume Studies Need a Different Approach

Low-volume studies demand subject-level oversight, where patient context and emerging risks matter more than population-wide trends.

Rethinking Safety Oversight in Small Trials

In small trials, the biggest safety signal may come from a single patient, if your oversight process is designed to see it.

RBQM is moving from concept to capability

RBQM adoption is widespread, but true risk-based monitoring maturity is still rare. Here’s what ACRO’s latest report reveals.

RBQM Success Stories

"Worldwide’s RBQM team is one of the most experienced CRO teams in the industry. This, coupled with TRI’s best-in-class technology, ensures we can proactively identify and manage risks, meaning improved quality and patient safety, and, in turn, provide a better experience for sponsors and patients."

"What truly set TRI apart from other vendors was their unparalleled commitment to a quality deliverable helping us effectively apply a novel approach to our operations. They achieved a deep understanding of our objectives by partnering with us on a rigorous change management process which culminated in a shared vision for the integration of their risk assessment and central monitoring solution."

"The Worldwide Clinical Trials team is pleased with our continued partnership with TRI and we are excited about the milestone of having 150 clinical trials in TRI's Risk-Based Quality Management platform. This is a key benefit for our customers as it improves data quality, trial efficiency, and patient safety."

"It has been such a wonderful ride with our TRI partners over the last few years developing our RBQM strategy with our Sponsors and Worldwide Clinical Trials Teams! We love working with everyone at TRI and look forward to bigger and better things to come!"