{ Clinical Development }

DaVita Clinical Research (DCR) has the patients and expertise you need in Phase IIb-IV renal studies

 

You know the value of experience when choosing a clinical trial partner to assist with Phase IIb-IV trials. No company offers the virtue of a greater depth of knowledge in renal research and clinical development than DaVita Clinical Research.

 

Our relationship with physicians, medical groups, and dialysis centers from coast to coast gives us seamless access to over 115,000 renal and specialty populations, allowing DCR to quickly fill and conduct trials — even those requiring unique patient populations. DCR also gives you access to the world's largest and highest quality ESRD clinical data warehouse — comprising 228 billion data points on over 115,000 patients — which is invaluable in feasibility and protocol design. For sample analysis, DCR leverages relationships with central laboratories across the nation to ensure accurate and consistent testing. DCR’s access to renal patients decreases your time-to-market costs and increases market opportunities.

 

Trial Management Services

DaVita Clinical Research assists you in all aspects of program development, including:

  • Development consulting

  • Site selection

  • Patient recruiting

  • Expedited start-up

  • Expert study management

  • Bioanalysis

  • Quality assurance

  • Data management

  • Regulatory affairs

  • Scientific writing

  • Publication support

Phase IIb-IV Studies

DCR’s 20-year track record of conducting broad-based national studies involving CKD and ESRD subjects is your assurance for efficient and effective trials.

 

Study capabilities:

  • Clinical efficacy

  • Safety and pharmacovigilance

  • Pharmacokinetics

  • Feasibility studies

  • Special populations

  • Periapproval studies

  • Post-marketing studies