Database build and Amendments on Any EDC platforms
Study build life cycle support and management by industry certified and experienced professionalsExplore…
for project management and development
Clinical Programming and reportingView More..
cross platform solution to manage your study build life cycleClick for demo
Radiant DataCare (RDC) is one among the specialized Clinical IT solutions and services company providing the best quality solutions to the clinical research industry. RDC takes the strategic approach in implementing solutions for the challenges involved in clinical data management, database build life cycle, clinical programming and data extracts. RDC understands the needs of having strong and experienced resources for designing and implementing clinical studies electronically.
RDC was formed by professionals who have more than 20years of industry experience on multiple EDC platforms. With all the great experience we know the needs of the clients and understand their challenges in bringing the quality clinical studies and manage. We work with our clients in each step and support them to manage the clinical studies and make sure they follow all the industry standards. All our teams are well trained on SDTM and CDASH standards and follow the CDISC standards.
With several years of Clinical IT experience RDC evolved with the unique processes which are mostly acceptable to the clients across the nations to associate and participate in the entire life cycle. With the latest simplified processes we have been successfully implementing clinical studies on the industry well known EDC platforms like Medidata Rave, Open Clinica, Acceliant and Inform. Our leadership’s industry experience in not only limited to the below Therapeutic areas. However the latest involvements are in Cardiology, Oncology and Medical device studies. We are further exploring into multiple Therapeutic areas in parallel.
You can reach us by clicking this link (Contact us).
RDC providing services with respect to clinical database management and programming not limited to:
Study Conduct and Database Build
Study Maintenance and Amendments
Database Lock and Submissions
SAS Data Extracts and programming
JReview and BOXI reporting
Project management support
StudyWIKI is a unique platform used to design clinical studies independent of any EDC platform. StudyWIKI facilitates an environment to create and maintain library of common study elements/objects that are independent of EDC tools. Library consists of Studies categorized based on Therapeutic areas.
It provides the unique eCRF design studio environment for creating and designing eCRFs easily by just drag and drop feature. The design studio also facilitates creation of Data Validations quickly and easily by selecting the rule elements in simple english.
The users can design eCRFs rapidly and can save more than 70% of time in creating specifications and study designs. The designed studies can be deployed into the EDC platforms of client’s choice (provided the EDC map is in place with the tool).