actON QbD Workshop | Episode 10: How do you keep QbD/RBQM on track during the trial?

actON QbD Workshop | Episode 10: How do you keep QbD/RBQM on track during the trial?

QbD/RBQM in a trial starts long before a participant is screened. It is trying to pre-empt issues and minimize them up-front. Once the trial begins, though, reality hits – new risks and issues emerge, some identified risks are not as great as were thought initially, and not all the risk controls may be as effective as planned. Risks and their controls need regular review. In this workshop, our experts, Keith Dorricott, Johann Prove, and Julien Nunes Goncalves, will discuss some emerging best practices in this area. We will demonstrate how Cyntegrity’s MyRBQM® Portal can simplify the review and keep it on track so that the risks to trial participants and data are always kept at a minimum.

What You Will Learn:

• How to continuously monitor and review risks throughout the clinical trial

• Strategies to adapt QbD/RBQM plans when new risks or issues arise

• The importance of dynamic risk control effectiveness assessment

• How Cyntegrity’s MyRBQM® Portal streamlines ongoing risk reviews and decision-making

Who Should Attend:

• Clinical Project Managers

• Risk and Quality Managers

• Clinical Operations Teams

• Data and Safety Managers

• Regulatory and Compliance Professionals

Why Attend?

Maintaining QbD and RBQM on track is essential to protect trial participants and data integrity. Learn practical best practices and how technology supports proactive risk management.

Don’t Miss This Workshop!

Join us and discover how to keep your QbD/RBQM processes agile and effective from start to finish in clinical trials.