CIMS Global has been providing innovative eClinical solutions for over 16 years. We have a modern, fully integrated & customizable software suite for the digital era. We are NOT JUST ANOTHER SOFTWARE VENDOR. In addition to CIMS eClinical solutions, we provide FULL DATA SERVICES including: • Biostatistics • SAS programming • Data management • Sample size estimation • Group Sequential Design • Dynamic Trial Design • Seamless phase 2/3 combination design • DDM planning, implementation and execution • Support Independent Data Monitoring Committee (IDMC) with DDM • FDA/EMA interaction about DDM With our proprietary closed system, we’re empowering pharmaceutical and biotech companies to bring drugs to market sooner, saving millions of dollars on clinical trials and bringing much-needed therapies to patients A Complete EDC / eClinical Solution Unlike Any Other on the Market The CIMSTM eClinical Suite is a cloud-based, fully validated, 21CFR11 compliant intelligent platform that enables users to intuitively manage the complexities of clinical trials by sharing consistent trial data across the entire trial process. This allows the sponsor to seamlessly manage trial processes, effectively deploy critical resources, proactively address performance issues and streamline operational workflows. Access comprehensive EDC modules (EDC, eTMF, CTMS, Randomization, Clinical Supply management, eSafety) connected to smart mobile apps to streamline the clinical trial process from study setup to regulatory submission. Dynamic Data Monitoring Stop hopeless trials early, continuously monitor and adapt potentially promising trials. Saves Time Saves Money An AI-engineered statistical package for monitoring clinical trial progress The CIMS Dynamic Data Monitoring engine utilizes machine learning and artificial intelligence (AI) technology in an integrated, closed system with EDC and IWRS.