Archives: Agenda

• Pre-implementation data and workflow challenges – A look at the inefficiencies and pain points in paper-based workflows and the impact on data management
• Navigating the implementation process – Key steps, challenges, and site engagement strategies for successfully transitioning to fully digital workflows
• Post-implementation impact: A transformative shift – How real-time oversight has reshaped workflows, improved data accuracy, and enhanced site operation

During the roundtable discussion session, the conference hall will be divided into zones. Delegates can choose which zone they would like to join. Each zone will be led by a table moderator and will focus on a different challenge within the running of an oncology trial in the US.

• Equipping patients with a better understanding of your trial to increase recruitment
• Modifying communication strategies to ensure patients feels fully informed with decision making and giving consent
• Incorporating health literacy in all stages of patient communication to ensure fully transparent clinical trials

• Navigate new regulatory requirements and complex study designs with larger sample sizes and a broader global footprint
• Implement country and site selection strategies that optimize FPI/LPI milestones
• Manage the complexities of enrollment, cohort management, safety review, and trial logistics across multiple regions
• Maintain a patient-centric approach to optimize study coordination and to benefit patienta

• Designing a protocol that adapts to increased complexities in trials to shorten timelines
• Creating adaptable designs that allows flexibility during trials for increased efficiency
• Strengthening foundations of your trial with a clearly defined protocol ensuring the collection of valid data