Menu
Redefine RTSM and EDC with simplified user-centric interfaces, making them more accessible and efficient for the end users
Intuitive interfaces that simplify trial
management for all users
Fully configurable and customisable to suit any trial design
Work with the Best in the Industry
What makes us stand-out is our expert knowledge of the IRT system. We have a team who have been solely dedicated their career to the IRT industry and have gained decades of experience in building the most complex studies.
No matter what your trial design requires, we have a team who can guide you and provide you the best solution at every possible stage of your clinical trail.
At ClinRT, we specialize in developing cutting-edge Interactive Response Technology (IRT) & Electronic Data Capture (EDC) systems.
Our mission is to revolutionize the clinical trial process by providing simplified and user-friendly interfaces, making IRT & EDC more accessible and manageable for sponsors and clinical trial sites.
Having collaborated extensively with clinical teams, we deeply understand the pain points faced by investigators and coordinators. With this insight, we’ve designed our IRT system to be intuitive, user-friendly, and visually appealing. Our multi-question page layouts enable investigators to complete all necessary inputs on a single screen, streamlining their workflow.
We recognize that sponsors need an IRT system that operates seamlessly, allowing them to focus on the more critical aspects of trial setup. Our system is designed for simplicity, offering quick setup and hassle-free management, freeing up valuable time for other priorities.
For CRAs, accuracy and clarity are paramount. Our IRT system provides an easy-to-navigate interface with clear and actionable data, empowering CRAs to verify site-entered information efficiently and effectively
Operating in a highly regulated industry, compliance is non-negotiable. Our system fully adheres to ICH-GCP, GDPR, 21 CFR Part 11, ISO 27001, CDISC/CDASH, and other essential regulatory standards, ensuring that authorities are confident in the data provided
ClinRT offers cutting-edge solutions designed to streamline and optimize your clinical trials. Our integrated IRT and EDC systems combine user-friendly interfaces with powerful functionality, ensuring efficient trial management, data integrity, and regulatory compliance. Whether you’re conducting a small study or a large-scale multinational trial, our flexible and scalable solutions adapt to your specific needs.
Our advanced RTSM system ensures efficient subject randomization and seamless drug supply management.
Electronic Data Capture Streamline your data collection process with our user-friendly and compliant EDC system.
ClinRT's IRT solution is fully configurable, allowing studies to be set up with minimal programming and shorter timelines.
Our setup uses pre-validated modules, ensuring a highly cost-effective IRT program. We do not charge for minor changes, such as adding countries or depots.
Our system is not only fully configurable but also fully customizable, allowing you to tailor it to meet specific protocol requirement
Our user-friendly system features a single-page, multi-question layout. Dynamic dashboards enable custom data exports through intuitive widgets.
When IRT changes arise, our expert project managers efficiently guide you through every step, providing optimal solutions.
ClinRT offers standard reports for site or study-level data, customizable for specific needs. To maintain blinding integrity, subject data reports are available in both Blinded and Unblinded versions, ensuring confidentiality while granting access to authorized users.
Our experienced project managers handle all study designs, guiding you from setup to completion. Support staff are available 24/7 across all time zones to assist with site queries.
Get in touch with our experts to discuss your specific needs
Head Office - London, UK
Other Branches : Hyderabad, India
