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BSI CTMS vs SiteVault CTMS

BSI CTMS

bsi-lifesciences.com

SiteVault CTMS

sites.veeva.com

Side by side

FigureBSI CTMSSiteVault CTMS
Price from—Free
Free plan—Yes
Free trial——
Open source——
WebYesYes
iOS—Yes
Android—Yes
APIYes—
Plans published12
Spec score · Clinical Trial Management7.5 (#2)7.6 (#1)
Spec score · Research Project Management Software7.5 (#9)7.5 (#10)
ComplianceBSI says CTMS is specified and validated for 21 CFR Part 11, ICH-GCP E6(R2), EMA/INS/GCP/112288/2023, and GDPR requirements.SiteVault states that it is GCP, HIPAA, and GDPR compliant and CFR Part 11 validated.
Founded19962007
HeadquartersBaden, SwitzerlandPleasanton, California, United States

Plans

BSI CTMS

  • BSI CTMSPriced on request

BSI CTMS pricing →

SiteVault CTMS

  • SiteVault FreeFree
  • SiteVault EnterprisePriced on request

SiteVault CTMS pricing →

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.

Visit bsi-lifesciences.com

SiteVault CTMS

SiteVault CTMS supports clinical trial management from pre-award budgeting and visit scheduling through invoicing and payment reconciliation after awards. It organizes study details, staff, milestones, pipeline, and workloads in one system. Customizable reports and dashboards show earned and forecast study revenue; automated tracking covers unbilled work, unpaid invoices, and invoice aging. Teams can see participant status, visits, and procedure completion in real time. The product is unified with SiteVault eISF and eConsent to reduce duplicate data entry, and Veeva says it connects with over 450 sponsors and CROs using Veeva technology. Free and Enterprise both list enrollment tracking, participant visit management, study budgets and Medicare Coverage Analysis, sponsor invoicing, and payment reconciliation. Free is free and includes 20 concurrent active studies; Enterprise offers unlimited active studies, an open API, SSO, and enhanced support, with price available on request. SiteVault states GCP, HIPAA, and GDPR compliance and CFR Part 11 validation. It is accessible from internet-connected computers, tablets, and mobile devices.

Visit sites.veeva.com