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

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

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

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

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.