October 9, 2025
August 20, 2025
The FDA has lifted REMS requirements for all approved CAR-T therapies, a move that could transform access for patients and research sites alike. What does this mean for trial participation, site activation, and the future of cell and gene therapy? Read on to see how this shift reshapes the CAR-T landscape.
August 20, 2025
Data entry continues to be one of the biggest sources of burden for sites. Electronic Health Record (EHR) to Electronic Data Capture (EDC) data transfer technology is a leading example of how sponsors, sites, and vendors are collaborating as an ecosystem to reduce the data entry bottleneck in clinical trial operations.
August 20, 2025
Improving the patient experience in clinical trials starts with supporting sites. Learn why Sponsors must prioritize the site experience to deliver better outcomes for patients and better results for the study.
July 22, 2025
June 23, 2025
Participant compensation is a critical factor in clinical trials, directly influencing trust, retention, and overall study success. Explore approaches that adapt to diverse needs, enhance experiences, and reduce operational strain, ensuring trials run efficiently while maintaining credibility and participant satisfaction.
June 23, 2025
Clinical research is no easy feat — balancing science, regulations, operations, and people is a high-stakes challenge. At the center of it all is the protocol, our guiding document. But more often than not, translating that protocol into real-world action feels like decoding a Rosetta Stone.
After reviewing more than 1,250 protocols, ProofPilot's Senior Clinical Program Manager, Kathryn Gentz, has identified six common mistakes that lead to confusion, deviations, and unnecessary costs. Here’s what to watch out for.
June 20, 2025
Behind every successful clinical trial is a site coordinator juggling chaos: patient care, payment issues, shifting schedules, and siloed systems — all while trying to maintain trust.
Read Emma’s story and see how Mural Health is reimagining site support by reducing admin overload, improving communication, and making participant management actually easier. Because when sites feel supported, trials succeed.
June 18, 2025
Manual transcription between EHR and EDC systems creates unnecessary delays, errors, and costs in clinical trials—with as much as 70% of the data being duplicated. Integrating these systems presents a powerful opportunity to streamline workflows, improve data accuracy, and accelerate trial timelines. Download a white paper showcasing how EHR-EDC integration can reduce site burden and help bring new treatments to patients faster.