IQVIA Virtual Trials enable hybrid and fully decentralized clinical studies, improving patient access and engagement while reducing site burden. With experience in 300+ DCTs across 50 countries, IQVIA combines technology, real-world data, and operational expertise to accelerate study start-up, enhance recruitment, and ensure data quality. The platform includes eConsent, telemedicine, patient diaries, remote monitoring, and mobile research staff to support home-based care. Configurable for global and complex studies, IQVIA’s approach improves timelines, expands geographic reach, and fosters diversity in participation. By reducing trial inefficiencies, IQVIA empowers sponsors to achieve faster, more cost-effective research outcomes.

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