ClinPlus
CTMS

eClinical tools that empower you to accelerate research and reduce compliance risk.

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 Benefits and Features of CTMS

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.

Anju Software + services are delivered on a unified platform which speeds deployment and offers unlimited options for your team.

Anju has developed technology solutions that enhance the value of its core vertical products.

LEARN MORE ON THE TECHNOLOGY PAGE

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.

Modules that extend base ClinPlus functionality and allow you to customize for your requirements:

ANJU CTMS

Clinical Trial Management System

CTMS is designed to help sponsors and CROs overcome the technical challenges associated with managing clinical trials.

More about CTMS

CLINPLUS EDC

Electronic Data Capture

EDC allows you to capture, monitor, clean and manage clinical data more efficiently to reduce the time to database lock.

More about EDC

CLINPLUS IWRS

Interactive Web Response System

IWRS services can be customized to provide the exact level of functionality required for you study.

More about IWRS

BIOSTATS TLF

SAS based Report Software – FDA Submission capable

BioStats TLF (Tables, Listings and Figures) is a statistical authoring tool for creating the highest quality safety and efficacy tables, listings and patient profiles.

More about Biostats TLF

CODING

Clinical Medical Coding Solution

As one of the most flexible stand-alone clinical coding solutions in the industry.

More about Coding

How can ClinPlus help your business?