Frenova site management works to strengthen clinical trials. 

As a dedicated site management organization, Frenova delivers a global network of research-ready sites, a diverse patient population, technology-enabled patient screening and enrollment, and expedited site start-up. Experienced Frenova staff are actively engage with all study stakeholders to enable key milestones to be achieved in a timely manner, meeting the highest standards and study requirements. From day one, you’ll work with a team that navigates the complexities that are vital to clinical trial success.

We work with sites to enroll the most suitable patients for renal clinical trials and studies of adjacent conditions, including, cardiovascular disease, diabetes, depression, obesity, or trials that involve rare diseases or vaccines.

Our relationship with Fresenius Medical Care enables us to grant access to potentially hundreds of thousands of ESKD and CKD patients worldwide.

Fresenius Medical Care is the world's leading provider of services for people living with renal disease, including more than 4,000 dialysis clinics throughout the world. Our relationship allows us to quickly identify appropriate sites and recruit patients based on the needs of the study protocol.

Frenova also offers data analytics and licensing services with access to one of nephrology’s largest longitudinal databases. It includes information on more than two million patients collected over 25 years by Fresenius Medical Care.

Frenova F1RST UP® sites in the US are up and running rapidly.


We use our deep experience to streamline trial feasibility, the IRB submission process, contracting, and budgeting. This helps you avoid the potential bottlenecks that can easily derail a clinical trial. 


Because we have long-standing partnership with physicians, patients, and the larger community, we can identify the most appropriate study participants for renal clinical trials and studies of adjacent conditions. Technology-enabled screening further advances the recruitment process.  


Our clinical project managers simplify site interactions and relieve administrative challenges associated with clinical trials. They anticipate and resolve issues, monitor progress and communicate directly with your team.