The SITC Biotech Regulatory Roundtable, held on Wednesday, Nov. 5, in National Harbor, MD, convened leading experts along with key stakeholders from industry and biotech to discuss pressing regulatory topics in immuno-oncology drug development.
Panels focused on FDA guidance initiatives, parent-child INDs, regulatory flexibility, and CMC optimization. An additional panel explored orphan and rare disease designations and regulatory pathways for rare disease drug development. The agenda closed with a panel on innovations in digital health, covering digital pathology, biomarkers and AI automation.
Designed for biotech innovators and IO stakeholders, this sold out preconference event offered a unique opportunity to engage directly with former FDA representatives.