Enhance patient safety and study quality by using data, analytics, and technology to monitor patient, site, and study performance with risk-based and centralized monitoring.
From emerging biotech firms to the largest global pharmaceutical companies, IQVIA's Connected Intelligence approach to Clinical Development helps you match the pace of innovation with integrated solutions and gives you the flexibility to match capabilities precisely with research needs.
We’re committed to providing solutions that help you innovate with confidence, maximize opportunities, and ultimately drive patient outcomes forward. IQVIA’s Connected Intelligence connects you to innovative trial solutions like precision site selection, centralized monitoring, automated safety case processing and global regulatory expertise.
Discover how risk-based and centralized monitoring can facilitate digital trial management and improve oversight, cost-effectiveness and patient safety.
Enhance patient safety and study quality by using data, analytics, and technology to monitor patient, site, and study performance with risk-based and centralized monitoring.
Harness the power of global human expertise combined with automation, artificial intelligence (AI) and machine learning (ML) to design, build and execute end-to-end safety solutions.
Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.
Create transparency in your regulatory documents with a range of medical writing services that deliver quality and timeliness throughout your product development lifecycle.
Getting the right outcomes from your clinical trials is all about the data and insights they provide. Biostatistics in clinical trials isn’t just a necessity, it can be a real competitive advantage.
Ensure you have access to insights early with connected devices and clean, analysis-ready data