Case Study: Oncology Company Achieves ~80% Acceleration in Gene Target ID/ Validation

Although data standards (e.g., CDISC) are mandatory for clinical trial submission to FDA, the data is often un-FAIR, limiting future reuse. The Pistoia Alliance FAIR4Clin guide explores the state of FAIR in the clinical space. In this session, Giovanni Nisato from the FAIR implementation Project emphasizes how this guide adds value to clinical data, accelerating research for data practitioners like clinical data managers or analysts. His session includes topics like metadata concepts and standards, clinical trial registries, clinical data quality, and governance.