Become a Sponsor of Choice with IQVIA Investigator Site Portal

Experience the difference of a complete study platform that sites are eager to use.

Make More Sites your Best Sites with the IQVIA Investigator Site Portal

See why so many companies have standardized their clinical operations on the purpose-built, proven platform that gives sites the power to succeed and sponsors the insights they need to improve performance and compliance.

Meet Clinical Trial Challenges Head On

Principal investigators (PIs) engage in clinical research to help their patients survive and thrive with the most advanced science and treatments. But PIs and their staff can quickly become overburdened with paperwork. Ironically, tech solutions imposed by sponsors often make matters worse, taking attention away from patients:

• Heavy administrative burden on investigators and sites
• Lengthy site activation and study start-up timelines
• Disparate technologies that reduce transparency and data quality
• Delays and frustration caused by manual processes and repetitive tasks

Investigator Site Portal

Start, conduct, and complete all your trials more effectively with IQVIA Technologies’ Investigator Site Portal, a collaborative platform designed to make life easier for sites and improve data quality. The Investigator Site Portal is composed of five modules and delivered in either a functional service provider (FSP) or software-as-a-service (SaaS) model.

Secure high-performing sites for all your studies

• Reduce administrative site burden
• Increase site satisfaction
• Decrease cycle times
• Increase data quality and transparency