Statistical Analysis

Versante provides expert statistical and analytical support that is second to none. We ensure appropriate statistical analysis and reporting that are consistent with the protocol and the statistical analysis plan. Our biostatisticians keep current with the latest statistical techniques in the literature, as well as those accepted by the FDA.

Clinical Plan Development

A comprehensive and insightful clinical plan that meets regulatory requirements is the key to successful drug development. Our team will work closely with you to optimize your clinical plan by exploring various strategies in order to shorten the total drug development time and/or reduce its cost.

CDISC Conversion

Versante has developed a proprietary tool that is used to efficiently transform existing and legacy SAS datasets into CDISC SDTM compliant formats and standards. Our solution offers a rapid, low cost and error-free alternative.

Data Management

Our qualified team of Statisticians, CRF Designers, Database Programmers and Data Managers all work together in developing the Data Management Plan specific to your trial. We have experience in working with paper-based data collection methods as well as with electronic data capture (EDC) systems.

Consulting

Versante clinical Research Solutions has set itself apart from its competition by establishing a sensitivity to clinical trials cost and preservation of the bottom line. This has made it a leader in the development of long-term relationships with industry clientele.

Clinical SAS Training

Versante Research Solutions is started by IT/Clinical Industry experts and well experienced software trainers. We are providing comprehensive training in SAS(Statistical Analysis Software) to get the Real time practical exposure for implementing the software Applications.