CTMS Master

CTMS Master is a clinical trial management system (CTMS) developed by Anju, designed to address technical challenges associated with managing clinical trials. It targets organizations seeking to improve user accessibility and communication, reduce manual operations, and eliminate redundant data entry and tasks across study projects, countries, and sites.

The platform supports end-to-end trial management, covering study setup, site visit reporting, finance and budget management, protocol deviation tracking, and informed consent monitoring. It integrates with Anju's TrialMaster EDC as well as third-party EDC, IVRS, and eTMF systems through an adaptive eClinical platform.

Key Benefits

• Integrated monitoring tools: An integrated Site Visit Report (SVR) tool with automated workflow eliminates duplicate data entry and supports the creation of out-of-the-box Site Visit Reports.
• Quick study setup: Standard templates for project and site documents, events, milestones, site visit reports, and budgets can be maintained and tailored for each individual study.
• Project insight and reporting: Provides over 100 metrics and statistics for clinical study projects, countries, and sites, along with more than 80 standard reports and ad hoc reporting capabilities.
• Study finance management: Supports defining site-specific budgets from a default budget template, tracking accrued payments and future obligations, configuring automatic or manual approval for each payment type, and producing invoices on behalf of investigators.
• System integration: Pulls key study metrics directly from TrialMaster and supports integration with other EDC, IVRS, or eTMF systems via Anju's eClinical platform.

Core Capabilities

• Informed consent tracking: Tracks informed consent versions and signature status to support quality and compliance requirements.
• Blogs and communications log: Tracks trial communications including emails, phone conversations, and miscellaneous information at the project, country, site, and enrollment levels, with optional linking to sites or subjects.
• Study finance and budget management: Defines site-specific budgets, tracks accrued and future payments, manages payment approvals, and generates investigator invoices.
• Quick study setup: Maintains customizable standard templates for documents, events, milestones, site visit reports, and budgets applicable across studies.
• Integrated Site Visit Report (SVR) tools: Uses standard templates to automate SVR creation, pulling in sections such as monitoring information, protocol deviations, serious adverse events (SAEs), action items, narratives, and more. An automated workflow manages SVR authors, reviewers, and approvers through email notifications and generates metrics from first draft through final approval.
• Protocol deviation management: Tracks both system-generated and manually entered deviations, with automated resolutions and tracking of corrective and preventative actions (CAPAs).

Related Products and Integrations

• TrialMaster: Anju's EDC system, with which CTMS Master has a direct integration for pulling study metrics.
• Trial Master File: A related eClinical product within the Anju portfolio.
• TA Scan: Described as an all-in-one clinical intelligence solution, also part of the Anju product suite.

CTMS Master is part of Anju's broader adaptive eClinical platform, allowing it to connect with external EDC, IVRS, and eTMF systems in addition to native Anju products. A personalized demo is available for organizations evaluating the system.