CTMS Master OnLight

Maximize Insights and Effortlessly Manage Clinical Trials

Premier clinical trial management system designed specifically to help overcome technical challenges associated with managing clinical trials. CTMS Master improves user accessibility and communication, reduces manual operations, and eliminates redundant data and tasks, allowing a more efficient trial conduct. 

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Benefits

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Fully Integrated Monitoring Tools

An integrated Site Visit Report tool with automated workflow eliminates duplicate data entry and facilitates the creation of out-of-the-box Site Visit Reports (SVR).

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Quick Study Set-Up

Maintain standard templates for project and site documents, events, milestones, site visit reports and budgets that are tailored as needed for each study.

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Excellent Project Insight

CTMS Master provides 100+ metrics/statistics for clinical study projects, countries and sites as well as 80+ standard reports plus ad hoc reporting capabilities.

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Study Finance Management

With CTMS Master, you can define site-specific budgets from a default budget template, track accrued payments and future obligations, define automatic or manual approval of each payment type, and produce invoices on behalf of investigators.

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Seamless Integration

View key study metrics pulled directly from TrialMaster through the seamless integration. Further, take advantage of Anju Software’s adaptive eClinical platform, allowing CTMS Master to be easily integrated with any other EDC, IVRS or eTMF systems you may have.

Key Capabilities

Maintain standard templates for project and site documents, events, milestones, site visit reports and budgets that can be customized for each study.

The CTMS Master SVR toolkit uses standard templates for automating SVRs. Pull in detailed sections such as monitoring information, protocol deviations, SAEs, action items, narratives, etc. An automated workflow guides SVR authors, reviewers and approvers through the process via email notifications and generates metrics from first draft through final approval.

Stay on top of both system-generated and manual deviations through automated resolutions and tracking of corrective and preventative actions.

Ensure quality and compliance through informed consent versions and signature status tracking.

Stay on top of trial communications through emails, phone conversations or other miscellaneous information. Blogs are available at project, country, site and enrollment levels and can be optionally linked to sites or subjects.

Define site-specific budgets from a default budget template, track accrued payments and future obligations, define automatic or manual approval of each payment type and produce invoices on behalf of investigators.