CTD
Clinical Trial Disclosure

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

Clinical Trial Disclosure (CTD) is a clinical trial platform designed for the regulated environment of Life Sciences. CTD automatically imports data from excel spreadsheets, internal systems and or public websites and shares common data across the structured forms. The configurable workflows, with email notifications, ensure the work is completed on time and captures all stakeholder actions. Just push a button to upload to clinicaltrials.gov and to your CTD REGISTRY. This disclosure platform helps sponsor, manage and track clinical trial disclosure content and the process that goes along with it. This is especially effective when dealing with global teams in terms of access from a centralized platform.

CTD can be deployed and ready to use within days. The system includes an integrated training module that assists with user on-boarding. The migration utility instantly downloads sponsor records from clinicaltrials.gov and EudraCT. The unique system configuration enables users to modify records quickly and get them approved for publishing including all the steps in between (authoring, editing, approving and publishing).

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

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