We provide our Clients/Partners with a full range of clinical data services in phase I – IV. From CRF design to final study report our team will bring their expertise to insure the quality and timeliness of our deliverables.

    Our data management group has experience in managing traditional paper based and EDC trails.  Combining the right technology and processes we insure timely and accurate database setup that is focused on insuring the quality and accuracy of your data. Our processes are designed to insure the  efficient use of resources and the timely lock of the clinical trial database.

    Our team of statisticians has the expertise to guarantee that the statistical plan will meet regulatory requirements. Our statistician involvement begins with the protocol development to insure that they can provide the strategic advice to optimize data analysis and that your protocol development is based on the correct statistical methodology and analysis.

    Our team of statistical programmers uses SAS software for all of the output requirements in support of the study report and statistical analysis. The statistical programmers are involved early with the statistician in the development of the analysis plan to identify potential data issues and develop data handling conventions for analysis. Programming validation is done following SDLC methodology.

    Our team of medical writing experts will use their extensive experience and expertise to insure that your documents and publications are delivered in a timely manner and of the highest quality. A clear and accurate clinical study report will insure the study understanding by all interested parties including regulatory agency and that the report will meet its objectives.