TCS Life Sciences Forum - An exclusive virtual series hosted by TCS ADD™
AI-driven RBQM for Improved Efficiencies and Compliance
Day and Date: Wednesday, February 26th, 2025
Time: 8:30 PM IST/4 PM CET/10 AM ET
Duration: 90 mins
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Life Sciences
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TCS ADD™
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TCS ADD™ is a suite of modern and open technology platforms for clinical research and drug development that helps make clinical trials more agile and safe.
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About the event
Optimizing efficiency across pharma, CROs, and research institutions with AI-driven RBQM
Risk-Based Quality Management (RBQM) is transforming the clinical trial landscape by improving collaboration, data quality, site monitoring, oversight, and operational efficiency. We invite you to our upcoming virtual event, “AI-driven RBQM for improved efficiencies and compliance,” part of the TCS Life Sciences Forum, an exclusive virtual series hosted by TCS ADD™.
In this virtual event, we will explore the transformative impact of RBQM to reduce delays, optimize processes, and accelerate time to market across pharma companies, CROs, and research institutions. A real-world case study from a leading pharma company will enable attendees to grasp practical strategies for implementing RBQM and driving better trial outcomes.
Why is this a must-attend?
- Acceleration of clinical trial timelines: Learn how RBQM speeds up timelines, enhances decision-making, and optimizes trial execution while improving collaboration between pharma, CROs, and sites.
- Reduced monitoring costs and improved data quality: Discover how RBQM cuts monitoring costs, ensures higher data quality, and strengthens sponsor-site communication for more efficient trials.
- Real-world insights from a leading pharma company: Listen to real-world insights from a leading pharma company on how next-gen AI-driven RBQM improved trial outcomes.
- Optimization of site and CRO operations: Uncover leveraging RBQM for enhanced site management and real-time data insights.
- Future of clinical trials: Explore how emerging technologies like AI shape RBQM’s role in clinical trial efficiency.
- Expert guidance on RBQM implementation: Utilize the opportunity to ask industry experts about successfully implementing RBQM in your clinical trials and improving outcomes.
Who should attend?
- Pharma companies
- Clinical research professionals
- Project and risk managers
- Clinical trial consultants
Join us for a thought-provoking virtual event that delves into RBQM’s potential to accelerate your clinical trial journey. For further details, please visit us on https://www.tcs.com/what-we-do/products-platforms/tcs-add/solution/tcs-add-risk-based-quality-management-platform or contact us at add.platform@tcs.com.
We look forward to seeing you at the event.
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