Skip to content
SPECIFICTION
Get listed

Clinion CTMS vs SiteVault CTMS

Clinion CTMS

clinion.com

SiteVault CTMS

sites.veeva.com

Side by side

FigureClinion CTMSSiteVault CTMS
Price from—Free
Free plan—Yes
Free trial——
Open source——
WebYesYes
iOS—Yes
Android—Yes
Plans published02
Spec score · Research Project Management Software6.9 (#18)7.5 (#10)
ComplianceThe CTMS page displays compliance references to FDA 21 CFR Part 11, HIPAA, ISO 9001, ISO 27001, GDPR, ICH, and EU Annex 11.SiteVault states that it is GCP, HIPAA, and GDPR compliant and CFR Part 11 validated.
PurposeClinion CTMS centralizes trial oversight for sponsors and CROs, with project tracking, monitoring, and financial management.SiteVault CTMS supports trial management from pre-award budgeting and visit scheduling through post-award invoicing and payment reconciliation.
SupportClinion lists [email protected] for customer support inquiries.SiteVault includes on-demand 24/7 global support at no cost; the FAQ describes phone, email, and chat support and training at no cost.

Plans

Clinion CTMS

No plans published.

Clinion CTMS pricing →

SiteVault CTMS

  • SiteVault FreeFree
  • SiteVault EnterprisePriced on request

SiteVault CTMS pricing →

In their own words

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.

Visit clinion.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