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LifeSphere® CTMS

Gain complete control over clinical trial process

LifeSphere® CTMS

Gain complete control over clinical trial process

Key Benefits


  • Integrates event-based planning into configurable monitoring plans
  • Increases control with real-time status, tracking, metrics and KPIs
  • Delivers robust integration capabilities via pre-built connectors and web services
  • Assists independent audits and study-close out processes with versatile export capabilities

LifeSphere® CTMS – Versatile Clinical Trial Management Solution

LifeSphere CTMS is a comprehensive and versatile clinical trial management solution (CTMS) that enables life science organizations to plan, track and control all tasks and activities related to the set-up, conduct and closeout of clinical trials.

A fully configurable CTMS software solution, LifeSphere CTMS provides complete oversight over all clinical trial activity, ensuring clinical trial transparency. Study set-up is facilitated by automating many core activities such as study planning, site assessments, investigator selection, enrolment planning, document distribution and site visit planning.

Built on industry best practices to streamline study conduct, LifeSphere CTMS lets CRAs track the status of all site documents, track patient visits, perform site monitoring, track clinical trial payments and route completed visit reports through an automated, workflow-driven review-and-approval process. At study closeout, study teams can store all final documents in the embedded electronic trial master file (eTMF).

LifeSphere® CTMS – Versatile Clinical Trial Management Solution

LifeSphere CTMS is a comprehensive and versatile clinical trial management solution (CTMS) that enables life science organizations to plan, track and control all tasks and activities related to the set-up, conduct and closeout of clinical trials.

A fully configurable CTMS software solution, LifeSphere CTMS provides complete oversight over all clinical trial activity, ensuring clinical trial transparency. Study set-up is facilitated by automating many core activities such as study planning, site assessments, investigator selection, enrolment planning, document distribution and site visit planning.

Built on industry best practices to streamline study conduct, LifeSphere CTMS lets CRAs track the status of all site documents, track patient visits, perform site monitoring, track clinical trial payments and route completed visit reports through an automated, workflow-driven review-and-approval process. At study closeout, study teams can store all final documents in the embedded electronic trial master file (eTMF).

Key Benefits
  • Integrates event-based planning into configurable monitoring plans
  • Increases control with real-time status, tracking, metrics and KPIs
  • Delivers robust integration capabilities via pre-built connectors and web services
  • Assists independent audits and study-close out processes with versatile export capabilities

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