At Prism, we specialize in phase 1/phase II specialty populations, and complex study designs. Our emphasis is on regulatory compliance, communication, planning, training and execution. We tightly manage capacity to avoid over-extension of resources for all research processes, and tightly regulate active competing trials.
Through the development of strong partnerships, we can offer turn-key service including: central laboratory, bioanalytical, biomarkers and other specialty testing in partnership with MEDTOX Laboratories, data management, statistical analysis and SAS programming.
• Regulatory services (central IRB)
• Source documentation creation
• CRF creation
• Data management (manual, remote, electronic data capture/transfers)
• Subject recruitment
• Summary reports