The Global Exposome Summit 2026 is an international event dedicated to advancing exposome science and its applications to public health, environmental research, and policy. Bringing together leading scientists, regulators, healthcare professionals, innovators, and stakeholders from around the world, the summit will explore how lifelong environmental exposures interact with biology to influence health outcomes. Key topics include human biomonitoring, omics technologies, data integration, risk assessment, precision prevention, environmental determinants of disease, and translation of exposome research into policy action. The scientific programme features keynote lectures, thematic sessions, panel discussions, networking opportunities, and collaborative workshops designed for a multidisciplinary audience. 

PARC will actively contribute to the Global Exposome Summit 2026 by presenting research that supports next-generation chemical risk assessment and evidence-based health protection in Europe. Sigrid Dekeersmaecker (Sciensano ↗, Belgium) will present the communication “Integrating genetic and epigenetic biomarkers into human biomonitoring for next-generation health risk assessment”, highlighting the role of advanced biomarkers in strengthening exposome-informed health assessments. Sarah Cherfan ↗ (ANSES ↗, France) will present the communication “Burden of disease attributable to chemical dietary exposome in French children: A total-diet multiple-exposure, multiple-outcome study”, addressing the health impacts of dietary chemical exposures and innovative methods to quantify disease burden in children. 

The Global Exposome Summit 2026 offers a unique platform for exchanging knowledge, fostering collaboration, and shaping the future of environmental health research. PARC encourages researchers, policymakers, and stakeholders to take part in this important event and engage with cutting-edge science that supports healthier lives and safer environments. Registration details are available through the official summit website ↗.