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Duncan Hall speaking at MCC Clinical Trial Risk & Performance Management Summit

Duncan Hall, TRI CEO and founder, is a panellist at the MCC Clinical Trial Risk & Performance Management Summit.  Duncan is taking part in the session on Risk Management Emerging Practices and the Impact of ICHE6(R2) Updates which covers the following topics: Current risk assessment practices Challenges with risk tools released prior to ICHE6(R2) Realigning methodologies to support review of…

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Duncan Hall speaking at CBI Risk-Based Trial Management Conference

Duncan Hall, TRI CEO and founder, is speaking at the CBR Risk-Based Trial Management and Monitoring conference in Philadelphia on the 8th November.  His session will cover Operationalizing Centralized Monitoring. “Are you challenged with implementing Centralized and Risk-Based Monitoring to become R2 compliant?  What if there was a quick and easy way to compare, monitor and manage all your…

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The R2 story – what is it, why it’s needed & why now?

Lots of people don’t understand what R2 is and why it’s needed. And unless you understand the fundamental reasons for its creation and adoption, it’s easy to dismiss it as ‘just more bureaucracy’.  But it isn’t.  It’s much more important than that, and here’s the reasons why. The way clinical trials are conducted has changed dramatically over the last…

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The best questions from 3 years of webinars and training

Over the past three years we’ve trained over 1,000 people in webinars, on-line training sessions and face-to-face sessions.  Most of that training has been done by Tammy Finnigan, our COO.  She’s the person ‘on the hook’ to answer when someone asks a difficult question.  Fortunately for us, she has a wealth of experience in Quality Management, Risk Based Monitoring,…

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Webinar: OPRA – technology that makes quality management and R2 compliance simple

June 21, 10:00am EDT / 3:00pm BST Free webinar: OPRA – making quality management and R2 compliance simple       This webinar showcases TRI’s OPRA technology platform.  Learn how OPRA supports central monitoring, RBM, quality oversight and reporting. Understand what’s new in the latest release of OPRA and what’s upcoming in the next release.    To Register, click…

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Webinar: A practical guide managing protocol risks

June 14, 10:00am EDT / 3:00pm BST Free Webinar: R2 readiness – A practical guide to protocol risk assessment, evaluation and implementing risk controls. This webinar is designed to help anyone planning to conduct protocol risk assessment and develop a quality management plan as part of ICH E6 (R2) compliance. The session will describe the regulatory context from ICH…

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Webinar: What you need to know about R2

June 7, 10:00am EDT / 3:00pm BST Everything you need to know about the key ICH GCP E6 (R2) changes. It’s for anyone wanting know what R2 is, why it has been implemented and how it will impact your company. The impact of ICH E6 (R2) on any company running clinical trials is going to be significant. With most…

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