Orchestrate better site-sponsor relationships
Increase transparency, improve communications and reduce administrative burden for all clinical trial stakeholders.
Meet complexity with simplicity
Even for the most experienced sites, starting up a new study is notoriously inefficient and inordinately burdensome. With protocols and regulations growing in complexity, it’s harder to recruit and retain patients and getting paid 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.
Transparency + Efficiency
The Digital 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.
- Eliminate redundancies inherent in the study-start process
- Provide complete transparency between sites and sponsors throughout the entire trial
- Free investigator and site staff to focus on patients
- Become a sponsor of choice
Reduce cycle time, speed site activation, and keep sites engaged with robust workflows and compliant eTMF filings
Improve site and sponsor relationships for more efficient clinical trials
