SUPPLIES

 

Global Clinical Supplies Management Solutions

In an era of improved Regulations to guarantee patient safety, Clinical Supply chain managers don't need to be warned of the things that can go wrong in their efforts to deliver supplies to many remote sites Globally in a Clinical Trial. Clinical Supplies strategy should be supported by automated systems to facilitate the process at the site and depots likewise offer more visibility across the supply chain, leading to better quality control.

DDi has 2 versions of IRT systems for Clinical Supplies. Both are Modular and Parameter based systems where each module is plug and play.

The Only system in the market which is Truly "No Build". All setup is performed in UI and it's flexible, user-friendly, reliable, and Regulatory compliant. This version will support about 70% of the studies and provide you industry best return on your investment.

Some of the Key Features and Benefits Include:

Quickest Go Live

Quickest Go Live

Our Go live time is Quickest in the industry with some studies made live less than 1 week

Adaptive Trials

Adaptive Trials

Having Supply setting capable of accommodating addition/deletion of Treatment Group or Kit Type at any point of time during trial is absolutely necessary in advanced IRT

Dynamic Help

Dynamic Help

A modern tool that has all the help menus with advices, alerts and information right there on the screen having less need to refer to a separate manual

24x7 Support

24X7 Support

Backed up by industry best Technical, Subject Matter Expert teams and Project Managers

All the reports, alerts and screens are tailored and tested to each user role. This is important to maintain the blind thought of the study. All documentation included in Compliance with Guidelines and Regulations.

Functionality included in XPRESS version:

Supplies Distribution

  • Inventory Release
  • Depot to Depot Transfer
  • Depot to Site Transfer
    (Manual & Automatic)
  • Expiry Date Management
  • Change Medication Status

Treatment Assignment

  • Randomization
  • Enrollment
  • Depot to Site Transfer
    (Manual & Automatic)
  • Expiry Date Management
  • Change Medication Status

Medication Assignment

  • Run In
  • Randomization / Enrollment
  • Scheduled Visits

For complex studies or studies where you need Company specific customization, our regular mIRT is provided which follows the route of URS, Build & Deploy with timelines ranging from 4 weeks to 7 weeks.

Features Include:

Robust Functionality

Robust Functionality

Custom Reporting

Custom Reporting

Direct to Subject

Direct to Subject (Partial and Full)

Able to handle

Able to handle sensitive Biologics

Compatible with Mobile

Compatible with Mobile

Can be integrated with any of the third party systems

Can be integrated with any of the third-party systems

Customized Dashboards

Customized Dashboards based on the role

Advanced Data Visualization

Advanced and self-service Data Visualization

Powered with eCOA ePRO

Powered with eCOA and ePRO

Medical Devices

Can be integrated with medical devices

IVRS

IVRS – Interactive Voice Response System

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Useful Resources

White Paper
mIRT

Clinical Supply Strategies to avoid Overages & Stock

Read More

Blog
Integration & Reconciliation IRT Guidelines

Integration & Reconciliation IRT Guidelines

Read More


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