How CTMS for Sites can organize and streamline your research
IBM CTMS for Sites has been in the marketplace for over 25 years as a site-facing clinical trial management system. It is a feature-rich and scalable platform used by institutions and organizations conducting research to streamline processes and help centralize clinical research operations and finances.
CTMS for Sites is designed to reduce financial compliance risk, increase performance transparency across organizations, maximize revenue or cost coverage, reduce the burden of duplicate data entry and support efficient participant recruitment.
Negotiate from a position of strength as a single site or for a network of sites.
Share operational insights through customized or standard reports, including one-click output to Microsoft Excel.
Understand your site's operational health with our real-time dashboards, and know that all of your data is secure with automatic backups and audit trails.
Access your system anytime via a web browser with product and technical support available 24x7x365.
Extend your clinical research management capabilities
- Manage study progress and finances
- Increase safety compliance with extended EMR integration
- Document coverage analysis and increase billing compliance
- Track patient visits and recruitment
- Determine operational health
- Budget, negotiate, invoice, and track payments
- Track time-based staff services
Security and privacy in the cloud
When using IBM Cloud offerings, your company can scale and adapt quickly to changing business needs without compromising security, privacy or risk levels. Learn more about IBM Cloud security
This offering meets the following industry and global compliance standards, depending on the edition you choose.
- EU-US Privacy Shield and Swiss-US Privacy Shield Framework
- ISO 27001
- SOC2 Type 1 (SSAE 16)
- SOC2 Type 2 (SSAE 16)
To learn about the compliance and certifications for a specific offering edition, consult the Cloud Services data security and privacy data sheets.