Join us for a thought-provoking virtual roundtable bringing together experts from across industry and academia to discuss the evolving role of omics standards in drug discovery, translational research, and clinical trials.
Speakers include:
- Bron Kisler – The Genomics and Omics Standards Landscape
- Adrian Czaban (Novo Nordisk) – CDISC Clinical Trial Use Case
- Dr. Jonathan Keeney (BioCompute / GWU) – Overview of BioCompute and FDA collaboration
The session will feature short presentations, live audience polling, and an interactive Q&A exploring key challenges such as interoperability, regulatory alignment, and adoption of standards across the R&D pipeline.
This roundtable offers a unique opportunity to learn how omics data and standards are shaping the future of biomedical innovation.
Register below