Innovation at ICON is focused on the factors that are critical to our clients. We develop integrated technologies to significantly enhance the efficiency and productivity of clients’ drug and device development programs, providing true transparency across all areas of a study.
An informatics platform to analyse the operational, clinical and real world data collected during clinical development.
Harmonising data and services for more integrated decentralised clinical trials.
Improving site selection and study start-up.
Digital solutions improving the clinical trial experience for sites, patients and study staff.
A cloud-based system featuring automated and configurable business rules to ensure regulatory compliance and provide visibility into the safety profile of an investigational product throughout its lifecycle.
Interactive Response Technology (IRT) platform for managing patient randomisation, investigator sites, and clinical supplies.
A central repository and analytic platform for all of your RWD assets.
ICON’s nonlinear mixed effects modelling tool, the industry standard for population PK/PD analysis.
PDx-POP is ICON’s software tool for expediting the iterative process of population pharmacokinetic modeling and analysis.
Streamling the management of images in clinical trials.
Sample Inventory Management System (SIMS) is an interactive reporting module in ICOLabs offering near real-time, high level traceability of all patient samples in a clinical trial.
PubsHub software streamlines and automates your medical and scientific communications and publication management.
ICOMaster is ICON’s electronic Trial Master File (eTMF) system. It offers clients secured access to files hosted on the platform. ICOMaster follows the TMF Reference Model, the industry standard file structure for TMF content.