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Free RBQM Resources
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TRI Blog posts on RBM and RBQM topics
Future Webinars on RBQM related topics
Webinar Recordings on RBQM topics
TRI guides and "how to" manuals on RBQM topics such as Risk Assessment in Clinical Trials
Videos from TRI on RBQM and Risk-Base Monitoring topics
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RBQM Ops 2022 - Day 1 Intro and Data Quality

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RBQM Ops 2022 - How does monitoring drive quality and efficiency?

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RBQM Ops 2022 - What does a good Risk Assessment look like?

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RBQM Ops 2022 - Day 2 Intro and Central Monitoring in Early Phase Trials

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RBQM Ops 2022 - How do we get to zero SDV?

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RBQM Ops 2022 - What does Good Central Monitoring Look Like?

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RBQM Ops 2022 - How big is the skills gap and what can you do about it

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Stats Basics - Getting to know your data

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What's great about the Funnel Model

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What's great about the Event Model

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RBQM Ops 2022 - Data Quality in Observational Research

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RBQM Ops 2022 - The participant journey in DCTs

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RBQM Ops 2022 - The Top 10 KRIs

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RBQM Ops 2022 - How central monitoring differs between early and late phase trials

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RBQM Ops 2022 - Key Considerations for Setting Up studies in Central Monitoring

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RBQM Ops 2022 - Learnings from the WHO Solidarity Findings

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RBQM Ops 2022 - Day 2 Panel session

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Duncan Hall, CEO, on why we developed OPRA 5

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Good Clinical Practice E-learning module

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Is it really different - How we use models and stats to help answer these questions

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RBQM Ops 2022 - What do the regulatory authorities really want to see?

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RBQM Ops 2022 - Implementing RBQM for Phase 1 Clinical Trials

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RBQM Ops 2022 - Day 1 Panel Session

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RBQM Ops 2022 - How do we identify and asses patients at risk?

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RBQM Ops 2022 - Do you trust data enough to make a decision?

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RBQM Ops 2022 - What roles and structures are required for end-to-end quality management

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RBQM Ops 2022 - How is monitoring driven by data source and collection?

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The origins of RBQM and ICH E6(R2)

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What's great about the TRI Operational Model

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Risk Assessment & Controls E-learning module