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    ClinPlus
    CTMS

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.

Key Features and Benefits

Quick Study Setup 

Create standard templates for project and site documents, events, milestones, site visit reports and budgets and modify as needed for each study.

Superior Document Management

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.

eTMF Harmonization

ClinPlus CTMS includes eTMF features to deliver a simplified, cost-effective process of managing, tracking and storing documents within a single system.

Fully Integrated Monitoring Tools

The calendar feature, integrated with Microsoft Outlook or any other calendars, allows project managers to view the project team’s schedule easily.

Excellent Project Insight

 More than 100 statistics, maintained for projects, countries and sites, may be included on the dashboard and in more than 80 standard reports.

Study Finance Management

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.

CTMS/EDC/IxRS Integration

ClinPlus CTMS supports web services technology to provide seamless, automatic integration with all popular EDC and IxRS products. 

CTMS Implementation

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.

ClinPlus product specialists are available to help bring the system to more efficient workflows.

KEY FEATURES THAT COME STANDARD IN CLINPLUS:

  • Single Sign-on/Single License
    Users such as CRAs who need access to both CTMS and EDC require only one ClinPlus license for true affordability.
  • Product specialists are available to integrate our systems with efficient workflows.
  • Protocol registration and clinical data disclosure.
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Contact Us      North America +1 877.468.6332      Europe +49 (0) 228 227 440      Click Here to Email Us

Contact Us
North America
+1 877.468.6332
Europe
+49 (0) 228 227 440
Click Here to Email Us