Blog24 September 2024 Unlocking FDA’s Vision for PRO Collection in RWE: Timing, Methods, and Insights Discover FDA’s guidance on collecting PROs for Real-World Evidence (RWE), focusing on timing, methods, and improving data quality. Learn more
Blog5 July 2024 Do We Still Need Patients in Tomorrow’s Trials? Modeling Placebo Effect and Beyond Discover the transformative role of AI in clinical trials, with expert insights from Derk Arts and MaryAnne Rizk on ethical and efficient drug development Learn more
Blog12 June 2024 eCOA: Afterthought or Essential Strategy? An Expert’s View on Choosing and Developing an eCOA Strategy The Evolving Landscape of eCOA in Clinical Trials Clinical trials have long grappled with the complexities of data… Learn more
