mIRT allows a user to implement a wide range of randomization methods and offers great flexibility with its fully validated randomization module. It supports all types of protocol randomization requirements to ensure balance, eliminate selection bias, and limit predictability.
Why Clinical Trial Randomization matters ?
Flexibility that Fits Your Needs
Implement simple to complex randomization schedules and algorithms depending on your protocol specifications and fully integrated and linked to Inventory. Leverage real-time randomization and notifications, blinded and un-blinded roles to control who can view your inventory and randomization events.
Confidence from expertise
When it comes to randomization, you need a solution provider with expertise to design and set up a functional and flexible solution that ensures patient safety. An experienced statistician will oversee the creation of your system and can advise you if needed on the options available to suit your clinical trial.
Customized to your trial
Each system is tailored to fit your trial so you only get the features you need (including simple, block, stratified, adaptive, biased coin randomization, minimization methods, Sequential Parallel Study Design (SPCD), and unequal randomizations). This makes the system easier to use by hiding unnecessary complexity.
Maintain Compliance
Our solution eliminates the risk of unblinding and adapts to changing site recruitment needs and maintains compliance with 21 CFR Part 11 to help clinical trials become more efficient, safer, and easier to submit to regulatory agencies.
Contact us to discuss how we can help you with a cloud-based fully validated randomization solution
The First Step
Let's talk about how DDi can help you