The objective is to harmonize the patient selection and sample processing. EPIVINF works with different cohorts established in three European countries and researchers will dedicate significant efforts to ensure that clinical profiles are comparable and controlled, but also that the samples are processed following comparable protocols. This is important so that the downstream analyses and results can be properly compared.
This WP also covers tasks related to data protection, ethics committee approvals and interactions with regulatory agencies to plan future development of novel strategies for personalized medicines.