{ Clinical Trial Management }
Expert know-how is essential to the successful management of late-phase clinical trials, and in renal research, DaVita Clinical Research (DCR) is unsurpassed. From protocol development through preparation of final reports, DCR professionals guide you through best-practice management techniques to ensure your trials result in successful regulatory submission.
Recruiting patients and clinical sites — often the most difficult part of a trial — is simplified by our extensive database of over 115,000 patients with CKD and other conditions, as well as our Clinical Network comprising 127 active practices and over 1,500 dialysis centers. With these as a starting point, DCR is able to quickly fill trials of almost any size with a broad range of patient populations.
A customized software system maintains and manages the planning, preparation, performance, and reporting, including budgeting and financials, patient management, investigator management, EC/IRB approvals, and compliance with FDA regulations.
The DCR biostatistics team clarifies the data and results of each study in addition to providing valuable study design and planning assistance across a range of therapeutic areas.
Finally, to help you prepare for final submission, our skilled and knowledgeable Medical Communication team gives your data the polish and clarity needed to proceed smoothly through the regulatory process.
