mindsON RBQM Workshop | Episode 35: Where does Quality by Design fit in?
The introduction of Quality by Design (QbD) in ICH E8(R1) marked a significant step forward in clinical trial quality management. But how does QbD fit into the broader framework of Risk-Based Quality Management (RBQM)? What is its relationship with Centralized Monitoring and Risk-Based Monitoring?
Join experts Johann Proeve and Keith Dorricott in this interactive mindsON RBQM Workshop as they share their insights on integrating QbD within RBQM practices. This session invites you to actively participate through live polling and collaborative whiteboards, or simply join to listen and expand your understanding.
What You Will Explore:
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The role of QbD in RBQM
Understand how QbD principles underpin risk-based approaches in clinical trials. -
Connecting Centralized and Risk-Based Monitoring
Learn how these monitoring strategies complement QbD and enhance trial oversight. -
Practical integration strategies
Discover ways to align QbD with your existing RBQM systems for improved quality and compliance. -
Interactive learning
Engage with peers and experts, sharing your views and questions in real-time.
Who Should Attend:
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Clinical Quality and Compliance Professionals
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Clinical Operations Managers
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Risk and Monitoring Specialists
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Regulatory Affairs Teams
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Anyone interested in advancing RBQM and QbD integration
Why You Should Attend:
Understanding where Quality by Design fits within RBQM empowers teams to design more effective, risk-aware clinical trials. This workshop offers a unique chance to gain expert perspectives and collaborate with the clinical research community on best practices.
Don’t Miss This Workshop!
Join us for a dynamic, interactive session that deepens your knowledge of QbD and RBQM. Whether you’re new to these concepts or looking to enhance your current strategies, this workshop will add value to your clinical trial approach.
