A large pharmaceutical company aimed to conduct a Phase IV post-marketing study with a streamlined randomization process using the in-house clinics of a US drugstore chain. The sponsor required a solution that would guide proper protocol execution for medically trained but research-naïve nurses and clinicians. Clinical Ink developed a large customized eSource study designed specifically for research-naive site end users. Learn more about this company’s experience in a free case study.
What you'll find in this whitepaper
- How Clinical Ink’s eSource platform streamlined randomization and R&D processes
- How a custom study improved data quality and created efficiencies for site personnel
- How electronic capture and storage eliminated the need for paper source