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

ClinPlus Electronic Data Capture (EDC) allows you to capture, monitor, clean and manage clinical data more efficiently to reduce the time to database lock. ClinPlus EDC study design is very fast and easy without programming regardless of the size, phase or complexity of your clinical trial.

Key Benefits of ClinPlus EDC

  • Supports risk-based monitoring
  • Provides customizable workflows for data entry, review, monitoring, signing and locking
  • Defines simple and complex edit logic without programming
  • Integrates seamlessly with ClinPlus Coding
  • Enables optional licensing of IWRS study by study to support simple and complex randomization schemes
  • Integration with ClinPlus CTMS is inherent and provides real-time trial management info and metrics to clinical operations
  • Allows users to easily define form groups and conditional form schedules
  • Provides flexibility with extensive configuration tools without having to rely on the software vendor

Key Features of ClinPlus EDC

  • Supports Multiple Languages
  • Advanced form table and form design tools
  • Comprehensive library of CDASH-compliant tables and forms and STDM code lists
  • Includes many standard data management reports, ad hoc systems and clinical data listings
  • Designed to be used in a 21 CFR Part 11 and HIPAA compliant environment
  • Enables you to manage global contacts, project and site teams
  • Role-based security and access controlled at the system, domain, project, country and site levels
  • Allows you to define tool-tips and author form-specific data entry guidelines and instructions
  • Complete in-line query management

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.



  • 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:


Clinical Trial Management System

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

More about CTMS


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


Interactive Web Response System

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

More about IWRS


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


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?