CompleWare Corporation is a leader in developing and providing electronic processes to capture and manage case report form (CRF) data, patient reported outcomes (PRO) data, and physiological data in clinical trials. CompleWare products and services allow sponsors to meet all of the goals of each clinical trial, from quick enrollment, to an increase in subject compliance, to rapid data lock, to a decrease in overall costs to meet the needs of the most challenging clinical trials. Experienced personnel are ready to assist with all aspects of clinical trials, including protocol design and drafting, collection and submission of IRB documents, monitoring, data management, centralized review of spirometry and ECG data, statistical analyses, and generation of final clinical study reports.
