BSI CTMS vs Clinion CTMS
BSI CTMS
bsi-lifesciences.comClinion CTMS
clinion.comSide by side
| Figure | BSI CTMS | Clinion CTMS |
|---|---|---|
| Price from | — | — |
| Free plan | — | — |
| Free trial | — | — |
| Open source | — | — |
| Web | Yes | Yes |
| API | Yes | — |
| Plans published | 1 | 0 |
| Spec score · Research Project Management Software | 7.5 (#9) | 6.9 (#18) |
| 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 CTMS page displays compliance references to FDA 21 CFR Part 11, HIPAA, ISO 9001, ISO 27001, GDPR, ICH, and EU Annex 11. |
| 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. | Clinion says CTMS connects natively with its EDC, RTSM, and eTMF products and can integrate with third-party EDC, RTSM, and eTMF systems. |
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.
Clinion CTMS
Clinion CTMS is a cloud-based, web system for managing clinical trial operations from Phase I through Phase IV. It centralizes milestones, site monitoring, and budgets for sponsors and CROs; Clinion also identifies study managers and site coordinators managing multi-site trials, timelines, or budgets as users. Milestone tracking compares planned timelines with actual progress and flags departures from the study plan. A centralized protocol-deviation log has dashboard filters and email notifications for events such as submission, review, and sign-off. Report and letter tools include templates, configurable approval workflows, action-item tracking, dashboards, and time-stamped audit trails. Financial features cover milestone-based invoicing and configurable site and vendor expense approvals, with recorded histories. Administrators can configure five-level approval hierarchies and more than 100 automated notifications and reminders. Clinion says CTMS connects natively with its EDC, RTSM, and eTMF products and can connect to third-party systems in those categories. Listed standards include FDA 21 CFR Part 11, HIPAA, ISO 9001:2015, ISO 27001:2013, ICH, GDPR, and EU Annex 11. Pricing is available on request.