Europe, Middle East & Africa
A more direct path to patients.
IQVIA Virtual Trials are bringing studies directly to patients at home. See how combining technology, data science, and clinical expertise speeds recruitment, heightens retention, and improves data quality – all of which helps you accelerate timelines and confidently achieve your study goals.
Trials designed around the patient
IQVIA Virtual Trials brings clinical studies directly to patients at home, creating a more human approach to clinical research. By designing trials around patients, participants are surrounded by support, improving recruitment and retention rates, and keeping study plans on track.
- Find the right patients faster. IQVIA’s patient recruitment platform uses real world data and analytics to find the patients you need, including diverse and difficult-to-recruit populations.
- Improve quality and patient safety. Virtual trials can reduce variation in data collection and provide near real-time data to enhance safety signal detection.
- Virtual is flexible. IQVIA Virtual Trials are scalable and flexible, and can be executed as full virtual or hybrid studies – large or small, local or global.
IQVIA Virtual Trials
The right technology to boost your study performance
At the center of our virtual trials solution is the IQVIA Study Hub™. Built on a highly secure, scalable SaaS platform, Study Hub enables orchestration of all study activities.
- Collect and disseminate data in real-time
- Communicate with patients via telemedicine, alerts, chat and phone
- Securely track IMP shipped directly to patients
- Centrally monitor studies
Powered by the IQVIA CORE
From local experts to renowned data scientists, unparalleled data assets to the latest in technology purpose-built for healthcare, the IQVIA CORE integrates everything you need to create a single, seamless virtual trial solution. Customized around your drug, patient population, and development stage, the CORE makes virtual trials a viable solution for you, today.
Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Access non-identified patient data with IQVIA’s device-agnostic platform that can provide both real-time data and endpoints.