Biostatistics Services
Biostatistics Services
Biostatistics Services
GVK BIO provides a complete range of development services to help clients progress their research programs through Clinical Research phases. GVK BIOs Clinical Biostatistics team offers statistical analysis for Phase II-IIIb trials. Our biostatisticians provide insight into trial design, develop complex statistical analysis plans and assist Sponsors through-out the regulatory filing process. Our experienced group of biostatisticians and programmers dedicate themselves to a project from inception to completion. We can serve as statistics experts for your trial or liaise with your companys internal statistics team to achieve your goals. Services Offered Statistical Inputs for Protocol Preparation Sample Size Calculation Randomization and Unblinding Procedures Statistical Analysis Plan SAS Programming using SAS 9.1.3 Validation of Biostatistical Programs and Outputs Statistical Report Writing Interim Analysis PK/PD Analysis Inputs to Clinical Study Reports Transactional Outsourcing We offer Biostatistics services for standalone deliverables such as Sample Size Calculation, Statistical Analysis Plan, Interim Analysis and other services listed in this brochure. These services are offered as a package of comprehensive support in all phases of clinical trials, as well as for preclinical studies in animals.
Business Model
Functional Outsourcing In this flexible business model, sponsors can choose GVK BIO Biostatistics team as their virtual Biostatistics department. The Clinical and Data Management leads within the sponsor organization liaise with our Biostatistics leads for full service statistical support.
Full Service Outsourcing As regulatory submissions require cross functional synergy between clinical operations, biostatistics, data management, and medical writing, GVK BIO offers integrated end-to-end services in these functions as a one-stop shop.
Biostatistics Services
Standards, Adaptability and Flexibility
Our Biostatistics team is adept at handling changes in client requirements and quick to adapt to the needs of the client, striving for satisfaction without compromising on quality or timelines. Can work in accordance with clients SOPs Collaboratively work with other CRO/Consultants statistician/ programmers Can work with ease with clients SAP and analysis standards Programming standards to meet client requirements Timely response for any additional or new requests Adaptable to changing needs during the course of the study Sound understanding of SDTM, ADaM and CDISC standards Our team is up to date with the latest statistical techniques accepted by regulatory authorities such as USFDA, EMEA and DCGI
Domain Expertise
HIV/AIDS Oncology Tuberculosis Leprosy Ophthalmology Pediatrics Malaria Diabetes Hepatitis Cardiology Multiple Sclerosis Dermatology Renal Impairment Psychiatry Quality of Life Sociological Studies PK / PD studies