Archives: Agenda
PANEL DISCUSSION: Future directions: Where will clinical data management be in 5 years and how should the industry prepare for its transformative potential?
- A roadmap to future proofing clinical data management: Implementing agile approaches to optimize stale workflows
- What will the growth of new clinical software vendors look like, and what will their offerings be?
- Scaling EDC and other systems to lead to the development of an integrated e-clinical environment and contribute to operational successes
- Ways in which today’s competitive pressures can push the industry to seek improved drug development strategies and shorten timelines
Realizing the value of data consolidation to maximize efficiency and improve processes
- Moving away from fragmented data and towards simplified pathways and what are the tools needed to facilitate data alignment?
- A look at Johnson&Johnson’s newly built platform to handle different data formats
- Ways to work together as an industry to hep standardize current processes
- Adapting to increased data sources and understanding the roadblocks to consolidating disparate data
- How can biotechs reliably minimize data risk and maximize data quality when combining different data sources?
Registration and refreshments
Chairperson’s opening remarks
Interactive Speaker-Hosted Roundtable Discussions
Interactive roundtable sessions offer a unique opportunity to come together with your peers to share best practice and develop solutions to critical challenges facing the industry as a whole. Each discussion will be led by a table moderator and will focus on a different challenge within rare disease clinical trials.
Roundtables are an exciting, interactive way to build your personal network and learn from the experience and expertise of others. After 45 minutes, delegates will have the opportunity to swap and choose a different table, and each roundtable will run twice.
Roundtable 1: Sharing experiences and highlighting importance of decentralizing in rare disease trials
Leila Cupersmith, Rare Disease Clinical Trial Expert & Patient Advocacy
Roundtable 2: Overcoming patient retention challenges in rare disease trials
Jenifer Waldrop, Executive Director, Rare Disease Diversity Coalition
Roundtable 3: Using new technologies in rare disease trials
Bruce Bloom, Chief Collaboration Officer, Healx
Morning refreshments and networking
Chairperson’s opening remarks
Registration and refreshments
Case Study: Discussing an approach to quality and clinical operations oversight in a rare disease trial at a small biotech
- Deciding the right level of oversight: key considerations
- Addressing communication hurdles and how to overcome them
- Supporting sites for operational improvement and inspection readiness