02.20.25 -- Automation Is Not Just AI

Unlock the potential of electronic Patient Reported Outcomes (ePRO) in your clinical research by implementing these essential best practices for success.

Creating new drugs or devices profoundly affects health and safety. See why it's vital for clinical research stakeholders — sponsors, CROs, and sites — to work together, meeting rigorous regulatory standards.

Industry experts share their perspectives on end-to-end clinical development, essential elements of a unified clinical platform, as well as the associated benefits and challenges involved.

Clinical trials are the backbone of pharmaceutical advancements, but they come with their own set of challenges, particularly in data management and supply chain logistics.

Around 200 trials annually use tools to measure the achievements of clinical remission. Implementing these in eCOA systems requires careful planning.