RBQM Training
with Industry Experts
Boost your quality management expertise with TRI's expert-led sessions, available in Beginner, Intermediate, and Advanced levels. Subscribe now to get the newest content straight to your inbox!
BEGINNER
Good Clinical Practice
Take our e-learning course to learn everything you need to know about;
-
Introduction to Good Clinical Practice
-
Understand GCP principles in relation to your role
-
Key GCP responsibilities for IRB/IEC & Sponsors
-
The importance of RBQM in clinical trials
BEGINNER
ICH E8 (R1)
Take our e-learning course to learn everything you need to know about;
-
Overview of the principles
-
Designing quality into clinical trials
-
Design elements and data sources
-
Study conduct, monitoring, and reporting
BEGINNER
Risk Assessment and Controls
Take our e-learning course to learn everything you need to know about;
-
RBQM and its importance in trials
-
Determining critical data and processes
-
Identifying and evaluating risks
COMPLIMENTARY TRIAL
Start Mitigating Risks Today!
Experience first hand how OPRA-RAM makes risk assessment and management simple for all clinical trials.
-
Complimentary 90-day trial
-
Drives ICH compliance
-
Easy-to-use cloud-based platform
INTERMEDIATE
Part 1/5: Defining Critical Variables
Join Kirsten McAulay, RBQM Operations Manager to learn everything you need to know about;
-
The intent of quality management
-
Regulatory background
-
Identifying critical variables
INTERMEDIATE
Part 2/5: Risk Identification
Join Macarena Sahores, RBQM Implementation Consultant to learn everything you need to know about;
-
Risk definitions
-
Risk identification
-
The risk statement
INTERMEDIATE
Part 3/5: Risk Evaluation
Join Kirsten McAulay, RBQM Operations Manager to learn everything you need to know about;
-
The intent of RBQM and quality management
-
Risk evaluation
-
Common risk evaluation misconceptions
INTERMEDIATE
Part 4/5: Risk Controls
Join Macarena Sahores, RBQM Implementation Consultant to learn everything you need to know about;
-
The intent of quality management
-
Risk control as part of the RBQM process
-
Common risk control misconceptions
INTERMEDIATE
Part 5/5: Risk Communication
Join Kirsten McAulay, RBQM Operations Manager to learn everything you need to know about;
-
Risk communication
-
Integrated strategic monitoring planning
-
Risk review and reporting
INTERMEDIATE
Top Key Risk Indicators for Sites
Join Duncan Hall, RBQM Subject Matter Expert to learn everything you need to know about;
-
KRI use cases and benefits
-
Using KRIs to support decision making
-
KRI's that are beneficial for sites
ADVANCED
Operationalizing RBQM
Join RBQM Subject Matter Experts to learn everything you need to know about;
-
What RBQM operationalization really means
-
Why operationalization is important
-
How technology can support operationalization of RBQM
ADVANCED
Making the Case for RBQM
Join Macarena Sahores, RBQM Operations Consultant to learn everything you need to know about;
-
What regulators are saying about CRF-based monitoring
-
How RBQM improves quality
-
the industry's hesitation in discussing cost savings
TESTIMONIALS
RBQM Success Stories
Hear directly from our partners about how we've helped them.
What truly set TriTrials 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.
RBQM NEWS
Clinical trial quality news and views
Subscribe to get the latest RBQM insights sent to your mailbox.
Dose Optimization in Oncology: Advancing Clinical Trial Quality through Risk-Based Approaches
The complexities of oncology drug development have long posed significant challenges, particularly in determining the optimal dose that balances therapeutic efficacy with patient safety. The FDA’s recent guidance on dose…
TRI Joins Veeva’s Product Partner Program
Partnership will drive quality and efficiency in clinical trials through enhanced risk-based quality management integration. [Cambridge, UK – 17.10.2024] – TRI, a leading Risk-Based Quality Management (RBQM) software provider for…
Risk-Based Clinical Data Management Takes Center Stage at SCDM 2024
The Society for Clinical Data Management (SCDM) annual conference has always been a cornerstone for clinical data professionals, but this year’s event, held in Boston from September 30th to October…