Biomarkers, CDx & Precision Medicine US 2026
Gaylord Pacific Resort & Convention Center, San Diego, CA
Biomarkers & Companion Diagnostics
PART OF BIOMARKERS, CDx & PRECISION MEDICINE US
23 - 24 September 2026 | Gaylord Pacific Resort & Convention Center, San Diego, CA
The Biomarkers & Companion Diagnostics programme covers the earliest decisions in the precision medicine decision chain: biomarker discovery and validation, CDx development, regulatory pathways for AI-derived biomarkers and AI/ML-based diagnostics, liquid biopsy strategies, patient stratification, and the oncology biomarker programmes currently being run inside the largest biopharma R&D organisations.
Across two days and three tracks per day, the programme sits alongside the senior US regulatory line-up on AI-derived biomarkers and CDx development. Cross-programme sessions then connect biomarker work directly to the multi-omics methods and computational pathology platforms operating around it, so delegates leave with a view of where their programmes fit inside the wider precision medicine landscape.

Hoifung Poon leads health AI research at Microsoft Research, focused on AI for accelerating biomedical discovery. His work spans foundation models for biomedicine, real-world evidence at scale, and how AI changes what biomedical researchers can do across the discovery-to-clinic pipeline. He opens Day 1 of Biomarkers, CDx & Precision Medicine US 2026 on AI for accelerating medical discovery.

A cross-programme regulatory panel brings Reena Philip (Executive Director, Regulatory Liaison CDx/IVDx, Merck), Karen McCullough (VP Oncology Regulatory Strategy, AstraZeneca) FDA representation into one conversation on what the agency actually expects from AI-derived biomarkers and CDx in 2026.
Track keynotes from Andrea Ferreira-Gonzalez (Virginia Commonwealth) on multi-cancer early detection, Hebe Sun (Regeneron) on the CDx regulatory framework in the US and EU, and Sapna Yadavilli (GSK) on preclinical strategies for clinical translation.
Plus sessions on liquid biopsy, patient stratification, oncology biomarker validation, and the operational reality of CDx co-development.


leading pharma, biotech, regulatory & academic delegates
Biomarkers & Companion Diagnostics Agenda at a Glance
DAY ONE
Track 1: Biomarker Identification, Qualification & Validation in Oncology & IO
Track 2: Companion Diagnostics & Regulations Track 3: Biomarkers in Translational & Clinical Development
DAY TWO
Track 1: Biomarker Identification, Qualification & Validation Across Therapeutic Areas
Track 2: Technologies for Biomarker Analysis Track 3: Biomarkers for Clinical Trials & Personalized Patient Treatment
Connect with 600+ senior pharma R&D leaders, translational scientists, multi-omics platform heads and spatial biology programme leads. 74% of delegates at the last edition were actively seeking new solutions, with over half with allocated budget.

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Position your company in front of the senior US biomarker and CDx audience: discovery leads, validation teams, regulatory voices and CDx programme heads from the largest biopharma R&D organisations. Sponsorship options include presentation slots, exhibition space, branded sessions and pre-arranged 1:1 meetings.
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Two days of senior R&D, regulatory and CDx conversations.
San Diego. 23 – 24 September 2026.
Key Event Highlights
An unmissable journey awaits you: from celebrated keynote speakers and insightful private roundtables, to an exclusive gala dinner. Discover the moments that will transform your NextGen Omics & Spatial experience.

