Better match investigators and sites to trial objectives
Meet complexity with simplicity
Even for the most experienced sites, starting up a new study is notoriously inefficient and burdensome. With protocols and regulations growing in complexity, it’s harder to recruit and retain patients, and setting up all the technology their expected to use takes a valiant effort. Many sites become so overwhelmed by the administrative burden that they withdraw after a single trial, further reducing the pool of investigators available for study opportunities from sponsors.
solutions
Industry-leading collaborations
Join the movement toward seamless site engagement with tools designed to lighten the load and boost efficiency.
Data Query System
One Home for Sites
Communicate key systems and workflow activities across multiple trials, connecting sponsors, CROs, and tech vendors.
SOLUTIONS
Site-focused technology
Solutions available independent of IQVIA CRO services to increase efficiencies and site satisfaction across your trials.
Feasibility
Improve and accelerate site vetting and selection processes.
Investigator Site Portal
Communication, collaboration and transparency between sites and sponsors mean trials start up and close out faster.
IQVIA SITE SUITE
Transparency + efficiency
IQVIA Site Suite puts the clinical research site experience at the center of your studies, where it belongs. These industry-leading and award-winning clinical applications give investigators, study coordinators, and site staff the self-serve access to information and documentation they need to run trials with the highest levels of patient focus, compliance and efficiency possible.
Built for sites to benefit all
IQVIA Site Suite delivers measurable impact across the clinical trial lifecycle. With high satisfaction, repeat usage, and significant time savings, it’s a platform built for site success.
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