Improve user accessibility and communications while reducing administrative burden
ClinPlus Clinical Trial Management System (CTMS) is designed specifically to help sponsors and CROs overcome the technical challenges associated with managing clinical trials. By improving user accessibility and communications, manual operations are reduced and redundant data and tasks eliminated, resulting in more efficient workflows.
Create standard templates for project and site documents, events, milestones, site visit reports and budgets and modify as needed for each study.
Electronic trial master file (eTMF) structures may be defined for document organization. Documents may reside in the CTMS database, Microsoft SharePoint or in a directory structure.
ClinPlus CTMS includes eTMF features to deliver a simplified, cost-effective process of managing, tracking and storing documents within a single system.
The calendar feature, integrated with Microsoft Outlook or any other calendars, allows project managers to view the project team’s schedule easily.
More than 100 statistics, maintained for projects, countries and sites, may be included on the dashboard and in more than 80 standard reports.
With ClinPlus CTMS, 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.
ClinPlus CTMS supports web services technology to provide seamless, automatic integration with all popular EDC and IxRS products.
ClinPlus CTMS system is installed preconfigured to common industry standards, while any client- and study-specific configurations are easily accomplished using system configuration tools without programming or vendor reliance.
KEY FEATURES THAT COME STANDARD IN CLINPLUS: