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Diagnostic Biomarker Verification and Validation: A Cost-efficient, Speed to Market Adaptive Design Clinical Trial Model
Session Chair(s)
Alan J. Touch
Chief Science Officer
Avodex Partners, United States
Clinical Trial Models for IVD Sample Collection and Human Factors Studies
Learning Objective : Discuss a cost-effective, time-sensitive sample collection protocol development using an adaptive clinical trial model that is aimed at establishment of the desired sensitivity and specificity algorithm for specific diagnostics continuing uninterrupted to a validation of use.
Speaker(s)
Clinical Trial Models for IVD Sample Collection and Human Factors Studies
Alan J. Touch
Avodex Partners, United States
Chief Science Officer
A Data Collection Strategy to Improve the Effectiveness and Speed of the Companion Diagnostic and Therapeutic Product Co-Development Process
Cari DeLoa
Genentech, A Member of the Roche Group, United States
Principal Data Manager
Future Outlooks for Imaging Clinical Trials in Latin America
João Massud, MD
Brazilian Society of Pharmaceutical Medicine (SBMF), Brazil
Senior Consultant, Drug Development
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