In conversation with Cristiana Campa: modernizing vaccine specifications and advancing risk-based quality frameworks
Vaccine Insights 2026; 5(1), 35–37
DOI: 10.18609/vac.2026.008
Published: 13 February
Interview
Cristiana Campa examines how advances in analytical characterization and risk-based regulatory frameworks are redefining vaccine development and manufacturing. Drawing on her work revising the ICH Q6 guideline on specifications, she discusses the role of harmonized, science-driven standards in supporting vaccine quality, global development pathways, and emerging modalities such as therapeutic and mRNA-based vaccines.
