Interactive Response Technology Clinical Trials Software Built for Flexibility and Scale
IXRS®3 IRT Solution
IXRS®3 is a market‑leading Interactive Response Technology (IRT) solution purpose‑built to streamline patient randomisation and clinical trial supply management across every study phase. Highly configurable and fully customisable, IXRS®3 supports simple to complex adaptive designs with real‑time, scientifically rigorous allocation methods, ensuring balanced treatment assignments, maintained blinding, and full regulatory compliance.
Backed by 24/7 global support from expert biostatisticians, language specialists, and system integration professionals, IXRS®3 delivers the reliability, scalability, and flexibility sponsors need to execute successful clinical trials worldwide.
IXRS®3 – Interactive Response Technology (IRT) Platform Fact Sheet
Download Almac IRT Fact SheetIXRS®3 Functionality for Modern Clinical Trials
IXRS®3
- Alerting
- Reporting
- Data Integration
- 24/7/365 In-house Technical Support
Subject
- Screening / Rescreening / Failure
- Randomisation / Enrollment
- Scheduled / Unscheduled / Skipped Visits
- Product Replacement
- End of Product / Discontinuation / Completion
- Codebreak / Safety Unblind
- Data Change / Correct
Supplies
- Supply Release Management
- Supply Ordering/ Automated/Manual
- Shipment Acknowledge
- Supply Edits/ Status/Location
- Resupply Strategy Management
- Expiry Management
- Depot Management
- ART / Account/Reconcile/Return/Destroy
Study
- Study Management/ Configuration settings/ Country settings
- Enrolment Controls / Open/Close/ Caps/ Cohorts
- User Management
- Site Management
Key IRT Features That Simplify Clinical Trials
IXRS®3 is designed to streamline complex processes and enhance usability for both sponsors and site teams:
Automation
Automates site-facing tasks to reduce manual errors and improve operational efficiency.
User-Friendly Interface
Empowers site users to make data updates independently – reducing the need for support and no risk to compliance.
Simplified Requirements Gathering
Visual tools replace lengthy documentation, making it easier to define and communicate study needs.
Controlled-Agile Development
Offers full visibility into each stage of the software build, enabling real-time feedback and eliminating surprises.
Pre‑Built Integrations
Comes equipped with ready-to-use connectors for commonly used third-party systems, with new integrations added regularly.
Testimonials
Startup Modes
IRT Boosters
Integration Partners
eClinical Solutions for Clinical Trials
Empower your clinical trials with cutting-edge eClinical solutions designed to streamline every step of the process. From secure and compliant eConsent to centralised data management through Almac One, and efficient visit management tools, our integrated platform ensures accuracy, transparency, and speed. Simplify complexity, enhance participant engagement, and drive smarter decisions with solutions built for modern clinical research.
