IBM Clinical Trial Management System (CTMS) for Sites, formally known as Merge Clinical Trial Management System for Investigators, is a platform used by institutions conducting research to organize, centralize, and manage clinical research operations and finances across their institution. It supports large hospitals and academic organizations as well as independent research organizations. When implemented as part of the central research infrastructure at clinical research sites, CTMS for Sites helps to streamline the clinical trial process and maximizes operational efficiencies. It is designed to reduce financial compliance risk, increase performance transparency across organizations, maximize revenue or cost coverage, reduce burden of duplicate data entry, and support efficient participant recruitment. CTMS for Sites provides a building block for centralization and standardization at research sites and can help create an end-to-end ecosystem that supports clinical care as well as research, regardless of research specialty or site type.
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections to deliver powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. Learn more at www.iqvia.com.
The Leader of Global Clinical Trial Management Sytems
RealTime Software Solution is a global leader in SAAS-based Clinical Trials Management Systems for Sites, Sponsors, and CROs. RealTime is also the only CTMS vendor that can offer a complete suite of solutions into a seamless platform, SOMS (Site Operations Management System).
SOMS includes the industry-leading CTMS, SitePAY, TEXT, eDOCS, and eSOURCE which is accessible through an easy-to-use MobileAPP. RealTime also has the most advanced multi-site and site network enterprise systems available anywhere.
With an international customer base, multiple integrations with other vendors, advanced recruitment systems, intuitive monitoring portals, Outlook integration, a powerful MobileAPP and more; the team at RealTime has made a significant impact on the efficiency of the clinical research process from start to finish.
Our History
RealTime-CTMS was initially developed in 2005 by experienced clinical research professionals. Today, the leadership and stakeholders of RealTime Software Solutions are some of the most prominent knowledge and opinion leaders in our industry. RealTime will continue to expand its service offerings and the delivery of disruptive new technologies that will shape the future of clinical research.
Bio-Optronics is the creator of Clinical Conductor (CC CTMS), known for generating significant savings with its robust finance capabilities, it is also the leading CTMS for executing collaboratively across multiple clinical trials and sites, including enabling remote workflows. Used by more research sites around the world than any other CTMS, Clinical Conductor is currently managing over 40,000 studies, including a significant percentage of the world’s COVID-19 clinical trials.
CC CTMS is part of the CCTrialSuite, a comprehensive set of integrated, patient-centric clinical research management products that together streamline research operations while maintaining a high degree of compliance. Complementing Clinical Conductor in the suite are several remote workflow enabling solutions. CCPay offers sites the unprecedented ability to both control finances and improve patient satisfaction with real-time payment reimbursements using secure pre-paid payment cards, all controlled remotely from CC CTMS dashboards. While CCText, the only fully CTMS-imbedded, conversational 2-way text messaging solution, has demonstrated clear results with increased patient recruitment, engagement and retention. An expanding set of remote workflow capable solutions include Part 11 compliant CCeReg document management, remote monitoring enabled CCeSource data capture, mobile friendly CCeConsent, and easy to engage remote visits using the HIPAA compliant CCVideo solutions from a single SaaS supplier, Bio-Optronics.
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Whether your priority is networking with sponsors and CRO attendees or learning best practices built for research sites, the Summit will provide a unique experience for your business.
For the last 16 years, the Global Site Solutions Summit has been committed to being “the site’s meeting.” The Summit provides a unique hub where sites, sponsors, CRO executives and regulators come together and share best practices, build their businesses, and develop new partnerships through debates, ideation sessions, workshops and focus groups.
SCRS is confident that by increasing site sustainability, all life science stakeholders will realize greater efficiency and profitability, and successfully meet our ultimate commitment to bring safe medical treatments to patients faster. The Global Summit will deliver the high-quality education, training, and best practices that attendees have come to expect.
BRANY was founded by the country’s leading academic medical centers in 1998, and has a stellar track record of working with community and academic hospitals and established investigators. BRANY understands the importance of high quality human subject research. In today’s increasingly complex study environment, we excel in helping IRB’s and hospitals continue to provide their patients with high quality clinical research. BRANY offers personalized customer service and project management, as well as ongoing communication through our quarterly newsletter and regular email updates
