iRIS | Laboratories

iRIS streamlines the collection, standardisation, and oversight of local laboratory data, helping sponsors improve data quality, reduce operational burden, and accelerate study timelines.

800+
Clinical trials
2.2 M+
Visits
62 M
Results

Challenges in collecting local laboratory data

Local laboratories play a critical role in patient care, but managing laboratory data across multiple sites, countries, and testing methodologies can create significant operational and scientific challenges. Missing data, inconsistent units and ranges, transcription errors, and variations between laboratories can introduce complexity that impacts both study oversight and downstream analysis.

For sponsors, these issues can lead to increased workload, delayed issue resolution, reduced confidence in datasets, and additional effort during database lock and regulatory submission preparation.

Global laboratory oversight simplified

iRIS helps sponsors simplify local laboratory data management through a centralised platform that harmonises results, improves data quality, and enhances study oversight.

Whether you're managing a regional study or a complex global program, iRIS delivers the transparency, consistency, and control needed to keep trials on track, delivering:

Improved data quality

Detect discrepancies earlier, standardise data across laboratories, and apply expert scientific oversight to identify issues before they impact study milestones.

Reduced operational burden

Free internal teams from resource-intensivedata management activities and allow them to focus on higher-value scientific and strategic priorities.

Accelerated study timelines

Access source documents electronically, resolve issues faster, and support more efficient progression to database lock.

Increased confidence in global data

Ensure laboratory values are harmonised and standardized across sites, countries, and testing methodologies, enabling more reliable analysis and interpretation.

Greater transparency

Access study metrics, transcription reports, laboratory results, and source documentation through a purpose-built, validated platform.

LabView360

IRIS is now integrated into LabView360, ICON’s unified digital platform for managing laboratory operations across clinical trials. By bringing together sample tracking, kit inventory, query management, and real-time reporting in a single environment, LabView360 delivers greater efficiency, visibility, and control for sponsors and sites throughout the clinical development process.

Embedded within LabView360, iRIS streamlines local laboratory workflows through intuitive electronic requisitioning, data capture, and query management. Available across multiple devices, it improves data quality and operational efficiency while reducing administrative burden. Built-in image capture and editing capabilities allow site staff to securely upload laboratory results and remove sensitive information within the platform, eliminating the need for time-consuming manual redaction.

From laboratory result to development decision

iRIS delivers the quality, consistency, and transparency sponsors need to manage global clinical trials with confidence.

iRIS streamlines the collection, standardisation, and oversight of local laboratory data, helping sponsors improve data quality, reduce operational burden, and accelerate study timelines.