Type 1 Diabetes
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.
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.
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.
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.
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.
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.
Versante Clinical Research Solutions Pvt Ltd., aspires to be a leader in providing drug development-related services to the pharmaceutical and biotech clinical-development stage-companies. Our team of proven experts in Biostatistics, SAS Programming and Data Management have extensive experience across a wide range of therapeutic areas. Work with Versante and benefit from shorter development times, enhanced product quality and reduced regulatory review cycles.
Versante’s expertise and services support all phases of clinical development programs. Our strategic planning creates synergies between our clients’ and our own expertise. Considerations that go into developing an optimal Clinical Plan include, but are not limited to, the following: available animal and human data, regulatory requirements, statistical rationale, clinical and ethical issues, and marketing needs. Our team consists of highly regarded industry professionals, with substantial drug development experience. Their diverse and rich backgrounds encompass careers with academic institutions, pharmaceutical companies, and CROs.
Every Versante team member is committed to outstanding quality, scientific integrity, delivery of projects on time and flexibility in addressing the changing needs of our clients. Driven by our passion to support the development of drugs that alleviate and eliminate disease, and leveraging our collective expertise, Versante will continue to lead the industry as the recognized expert.
Versante intends to be your expert virtual CRO, with a focus on providing innovative study designs to overcome complex challenges created by conflicting regulatory, marketing, medical and statistical needs, Versante is fully committed to delivering exceptional value to our clients.
Type 1 Diabetes
3JB, VJ Business Center,
GRG Layout, Trichy Road,
Coimbatore - 641 018
0422 - 495 2297
Mon - Fri, 9:00-18:00