This comprehensive track covers the latest advances in clinical research. It will provide updates on key developments on the Clinical Trial Regulation, the Clinical Trial Information System, data submission, transparency, navigating ethical approval, study design in the digital age, innovative clinical trial designs (umbrella and platform trials), digital tools in development and other hot topics. It should be a must-attend for optimising development programmes and identifying cost savings through efficiency and innovation.
Who is This Track Designed For?
DIA recommends this track and associated sessions to professionals involved in research and development, evidence generation, protocol development, study design, biomarker development, project management, patient centricity, statistics, clinical regulatory professionals and clinical assessors.