As a Frenova F1RST UP site, you would be a part of a network of premier research sites.  

Clinical trials have become increasingly more complex and demanding over the years. Frenova resources and designated infrastructure are designed to help navigate this complexity.

Our regional F1RST UP staff are dedicated to providing the best support for renal clinical trials and studies of adjacent conditions. They engage with pharma sponsors and CROs and deliver a range of technology-enabled, centralized services that help facilitate rapid start-up.

Frenova sets the standard for clinical and administrative support.

From day one, our team helps your team build the right infrastructure, define job roles, and conduct training on a variety of topics, including GCP, and relevant standard operating procedures, research and financial management.

Once recruitment begins, your Frenova clinical research coordinator will help accelerate screening and enrollment.

Our suite of proprietary tools and master agreements streamline the complexities of study feasibility, the regulatory process, contracting, and budgeting.

Throughout the life of your study, Frenova’s clinical project manager consults with your staff, monitors progress, and communicates with the study sponsor.

See what it takes to become a F1RST UP Site