CTIS is a government contractor with vast knowledge and expertise in how to develop and deliver cutting-edge IT solutions to meet specific needs in the healthcare space. We have a long-standing relationship with the National Institutes of Health, especially the National Cancer Institute, the National Institute on Minority Health and Health Disparities, and the National Institute on Allergy and Infectious Diseases, and we continue to build new relationships at NIH and in other federal agencies.
CTIS is working on the Inova Intelligence Informatics Engine (i3E) project, helping to optimize communications and increase interoperability among the various departments that serve patients. CTIS is also establishing a clinical data repository that will be available to all members of the hospital and clinical staff, thus eliminating hundreds of duplicate records and redundant expenses.
CTIS collaborated with Moffitt Cancer Center to implement and test the mobile and wireless technology software Safety Profiler, which is an adverse event management tool developed to improve the accuracy and efficiency of clinical trials staff.
CTIS developed registries as well as web-based portals for Washington Hospital Center, which facilitates connectivity, communication, and information-sharing processes, in order to reduce information and decision-making fragmentation. CTIS also developed the Institutional Review Board (IRB) document management system for MedStar’s Georgetown Lombardi Cancer Institute and Washington Cancer Institute (WCI), providing expedited IRB approval to conduct clinical trials.
CTIS has partnered with Georgetown University in building Institutional Review Board (IRB) management software and clinical research projects in the areas of translational and nanotechnology for National Institutes of Health (NIH).
CTIS developed a web-based portal to integrate and interface communication and collaboration between international clinical trial sites for CCGHE. CTIS also developed a scalable portal framework that promotes collaboration and document management and allows for data repository, including vital signs and metrics, for The Pneumococcal Vaccines Accelerated Development and Introduction Plan (PneumoADIP) project that was awarded by Global Alliance for Vaccines and Immunization (GAVI).
CTIS developed an Electronic Data Capture (EDC) system for University of Colorado Cancer Center (UCCC). This system is a case report form built to provide cancer clinical trial support at the site level.
CTIS is an information and communication technology (ICT) partner of INCTR. We have provided a worldwide, web-based portal that connects stakeholders domestically and internationally. CTIS developed an Electronic Case Report Form (eCRF) and a clinical trial data management system for the treatment of Acute Lymphoblastic Leukemia (ALL) in children and young adults. Four centers participated in the treatment of an ALL study group consisting of 450 patients.
Our firm created a Survey Management System (SMS) for a pilot study in India. We also developed a portal-based dashboard that allows monitoring, evaluation, tracking, and surveillance.
CTIS developed a Patient Management and Monitoring (PMM) system for 14 government facilities in Nigeria. This system contributed to the Global HIV/AIDS Initiative in Nigeria (GHAIN) and AIDS Care and Treatment in Nigeria (ACTION). We also created a data collection interface for clinical forms. This tool was delivered on laptops to physicians and patients in Nigeria.
Working with GAVI, CTIS developed a portal framework for the Network for Surveillance of Pneumococcal Disease (NetSPEAR) project in Eastern Africa as well as the International Centre for Diarrheal Disease Research (ICDDR) Project in Bangladesh. This framework supports information exchange between surveillance sites, helping to monitor diseases.
The Oncology Therapeutic Area (TA) at Novartis Pharmaceuticals is charged with the conduct of from 50 to 100 clinical trials each year. The majority of these trials are conducted under contract at remotely located extramural facilities. The use of traditional paper-based Case Report Forms to organize and document trial results led to delays of as much as six months in the availability of clinical toxicity data at Novartis. Early notification of efficacy data (e.g. tumor response) was not possible, presenting a decision barrier regarding further development of these drug agents. CTIS designed and developed the Early Development Infomatics Summary Over the Net (EDiSON) System for Novartis. EDiSON has increased trial efficiency by 30%. It has allowed Novartis to achieve higher institutional accrual and performance, and gives TA staff real-time access to clinical toxicity and early notification of efficacy data to effectively monitor trial progress.
CTIS provided GSK with the clinical trial patient summary data capture component, for use by investigators at clinical trial sites and GSK management. This offering is part of TrialBridge solutions, a custom web based framework for managing clinical trials data. This component provided capability for GSK to acquire, store and manipulate patient information related to participation in clinical trials. In addition, CTIS conducted training to GSK staff, setup the protocols, and provided helpdesk support.
CTIS assisted the UHG in defining Intelligent Data Fabric (IDF) technical and business models. This included delivering technology and vendor independent view of solution, design document articulating the high-level architecture and technical components required for the solution, define/capture the business value and high level use cases etc.
CTIS generated and distributed clinical data reports (Adverse event expedited report, Document milestone report, Response and AE Report/response and toxicity report) for the study under legal authority and approval from NCI to do as such.
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