Connected Devices

Augment trial data with digital 
endpoints

IQVIA Connected Devices experts streamline the selection and deployment of digital medical devices to collect and analyze data, simplify site workloads, and improve the patient experience.

A complete ecosystem for managing device data

The growth in biomarker data and study complexity requires vendors with the domain experience, applications, and global capacity to conduct clinical trials at scale.

IQVIA Connected Devices provide comprehensive patient-centric trial services that encompass device strategy with unbiased selection, scientific and therapeutic area expertise, best-in-class technology platforms, operational acumen, and dedicated end-to-end support.

Superior data capture and quality

High-quality management of continuous data across endpoints that meets regulatory requirements and improves study outcomes.

Flexible and future-ready solutions

Device strategies and configurable solutions that incorporate novel biomarker technologies and adapt to changes in the trial landscape.

Exceptional stakeholder experiences

Our teams build authentic partnerships with sponsors and sites to deliver more efficient, patient-centric trial experiences.

Partner with IQVIA Connected Devices

We earn our customers’ trust at every trial stage –advising on protocol design, addressing issues proactively, and streamlining operations to reduce risk and enhance study conduct.

IQVIA CLINICAL ESOURCE PLATFORM

Capture richer digital endpoint data

The IQVIA Clinical eSource Platform meets the new demands of the market by streamlining data collection, integration, and analysis. This study management solution also offers a real-time view of patient data that integrates other trial endpoints from virtually any connected device.

Once programmed to meet the needs of your specific trial requirements, the Clinical eSource Platform eliminates the guesswork from running all phases of clinical trials by fully automating each step within your workflow with meticulous precision and accuracy.

Whether you choose to fully automate your clinical trial—or choose to integrate real-time bi-directional data exchange to augment your current EDC solution—the Clinical eSource Platform allows you to harness the power of a truly paperless eSource solution.
The Clinical eSource Platform captures and analyzes data at the edge with enhanced speed and accuracy across all phases of clinical trials. Its unique ability to accommodate any connected device irrespective of its modality enables real-time bi-directional data exchange of the highest quality–in a true eSource solution that is 100% paperless.
This Platform eliminates the need for paper across clinical trials of all phases by seamlessly introducing connectivity and automation. By reducing the demands put on participants and clinical researchers, protocol adherence is maximized—resulting in higher quality, real-time data collection.
The Clinical eSource Platform is powered by intricate layers of granular data that drive and capture step-by-step processes for study coordinators, principal investigators, other site personnel, and CRAs, providing superior transparency and oversight that enhances inspection readiness.
2,500+

clinical trials supported since 1995

100%

IQVIA participation in US approved GLP-1 drug trials

35

therapeutic areas supported by IQVIA Connected Devices

335K

IQVIA Connected devices deployed in clinical trials

74K

site activations in 114 countries over the past ten years

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