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.
Veeva is the global leader in cloud software for the life sciences industry, serving more than 1,100 customers, ranging from the world’s largest pharmaceutical companies to emerging sites. As a Public Benefit Corporation, Veeva is committed to balancing the interests of its customers, employees, shareholders, and the industries it serves. Learn more at veeva.com.
Veeva SiteVault is the only unified solution connecting sites with sponsors and patients to run digital trials. Streamline regulatory processes and connect to 400+ sponsors that use Veeva Clinical applications. Learn more at sites.veeva.com.
Clinical.ly provides differentiated technological solutions to the clinical research industry, helping research facilities focus on conducting studies as efficiently as possible. We’re working hard to provide modern, intuitive software that frees up resources and reduces headaches. As trials keep evolving in complexity, it is becoming more apparent that the same old procedures aren’t keeping up. Inspection findings are much more costly than adopting the right technology, procedures and best practices.
The clinical trials industry is ready for better tools to help stay ahead of the evolving demands of sponsors and regulators.
We work closely with clinical trials facilities to understand their SOPs and provide solutions to help address their nuanced needs. By integrating your proprietary workflows, we help remove barriers to adoption and help you focus on your primary responsibilities. Free your medical staff to focus on the jobs you hired them to do.
eRegBinder by Clinical.ly is a purpose-built solution designed to help organizations meet regulatory compliance requirements in clinical trials. The system reduces mistakes by tracking required documents, signatures, and timelines, as well as offering automatic alerts on missing data. With electronic delegation and training logs, and remote monitoring access your time spent on regulatory compliance is minimized, helping you avoid spending employee time on fixing mistakes, omissions or missing information.
Save time and simplify your regulatory tasks with Complion, the industry’s leading eRegulatory solution designed to make your life easier.
• Eliminate paper binders
• Collect eSignatures
• Track expirations and outstanding tasks
• Ensure 21 CFR Part 11 Compliance
• Standardize filing and naming conventions
• Simplify remote monitoring
Experience the Complion Difference
• Trusted by 80+ sites to manage over 4,000 studies.
• Accessed by 1400+ monitors from 170+ sponsors and CROs!
• The only system designed to automate repetative tasks
• Best practices and industry standards
• Template policies and SOPs to ensure your long-term success
• Maximize sponsor acceptance and reimbursement
• Largest and most experienced team on the market
Sign up for a free demonstration today!
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.
Syneos Health is the only fully integrated biopharmaceutical solutions organization. Our company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry leading companies – INC Research and inVentiv Health – we bring together more than 21,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. To learn more about how we are shortening the distance from lab to life visit SyneosHealth.com.
