02.28.25 -- Optimizing Storage Solutions For Allogeneic iPSCs

This guide to clinical trials explores the regulatory approval, study startup, and trial processes essential for advancing medical innovation.

In addition to codifying some best practices, R3 recommends that sponsors adopt an approach to identifying and managing areas of risk to mitigate potential issues and enhance overall success.

Oncology clinical trials face unique challenges in patient recruitment and retention due to barriers such as awareness, logistical constraints, and eligibility criteria.

Real-world data (RWD) is increasingly vital for advancing breast cancer research, and leveraging TA datasets allows researchers and clinicians to address pressing challenges.

Discover how embracing fast and flexible clinical analytics can help you address clinical questions and provide real-time insights into data issues as they arise.