BSI CTMS vs Trial Interactive CTMS
BSI CTMS
bsi-lifesciences.comTrial Interactive CTMS
trialinteractive.comSide by side
| Figure | BSI CTMS | Trial Interactive CTMS |
|---|---|---|
| Price from | — | — |
| Free plan | — | — |
| Free trial | — | — |
| Open source | — | — |
| Web | Yes | Yes |
| iOS | — | Yes |
| Android | — | Yes |
| API | Yes | — |
| Plans published | 1 | 0 |
| Spec score · Clinical Trial Management | 7.5 (#2) | 6.8 (#5) |
| Spec score · Research Project Management Software | 7.5 (#9) | 6.8 (#20) |
| Compliance | BSI says CTMS is specified and validated for 21 CFR Part 11, ICH-GCP E6(R2), EMA/INS/GCP/112288/2023, and GDPR requirements. | The product page says the platform is designed to support 21 CFR Part 11, EU Annex 11, GxP, GDPR, and HIPAA. |
| Founded | 1996 | 2007 |
| Integrations | The vendor lists standard interfaces for Veeva eTMF, EDC systems, portfolio and project management tools, clinical data warehouses, and Active Directory single sign-on. | The product page lists integrations with EDC, IXRS, payments, eTMF, site portal, study start-up, learning management, and content management. |
| Reporting | Users can create customized reports from CTMS data and export them to Word, Excel, or PowerPoint. | Users can configure reports and dashboards with custom fields and monitor enrollment, milestones, activities, deviations, and safety signals. |
Plans
In their own words
BSI CTMS
BSI CTMS is a cloud-delivered clinical trial management system for pharmaceutical, biotechnology, diagnostics, med-tech, contract research, and academic organizations. Its unified platform combines CTMS functions with an electronic trial master file, study startup, and trial supply management. Teams can plan studies, track milestones, follow recruitment and randomization status, monitor sites, manage investigators, and record issues. The eTMF handles document creation, review, approval, electronic signatures, version management, and study-partner access. Risk-based monitoring, monitoring-visit workflows, offline monitoring, and an integrated learning management system support oversight and training records. Users can build reports from CTMS data and export them to Word, Excel, or PowerPoint. Listed interfaces cover Veeva eTMF, EDC, portfolio and project management, clinical data warehouses, and Active Directory single sign-on. BSI says the system is validated for specified clinical-trial and privacy requirements. Pricing is on request.
Trial Interactive CTMS
Trial Interactive CTMS brings portfolio, study, site, and subject data into a system for planning, monitoring, and reporting clinical trials. It is designed for sponsors and CROs, with workflows for CRAs, study managers, and clinical leadership. Planning tools include reusable activity plans, milestones, timelines, and country and region management. For site oversight, teams can use dashboards, schedule visits, review visit reports, track protocol deviations, and manage follow-up activities. Visit tracking also covers visit windows, required protocol activities, and informed consent form status. Configurable dashboards and custom fields support reporting on enrollment, milestones, activities, deviations, and performance indicators. The CTMS connects with built-in eTMF and a site portal for handling essential documents with an audit trail, and lists integrations with EDC, IXRS, payments, and other eClinical systems. The Site Visit and Trip Monitoring app works offline on Android and iOS. Platforms listed are Android, iOS, and web; deployment is cloud. Pricing is on request.