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About us

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About Us

We Are Providing
Best Service Since
2001 to present

VClincial Biostats is a global Contract Research Organization (CRO) based out of Austin, Texas that aims to provide Clinical SAS programming support. VClincial Biostats specializes in clinical data standardization for Phase I through IV Clinical Trials and is also involved in other regulatory services related to pharmaceutical product development. VClincial Biostats's strong beliefs and values define what we stand for and determine how we work. We have all the resources needed to analyze data obtained from Phase I through Phase IV clinical trials. Our expertise encompasses understanding the design of the protocol, recruiting patients effectively, managing the entire regulatory approval process efficiently, and making timely deliverables without constraining the client’s budget. Additionally, we stay up to date with rapid developments in the corporate arena and continuously review and upgrade ourselves to address these changes in the most effective manner.
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Our Team

We are currently a team of 10 members having around 3 years of end to end experience on average in Clinical SAS. As a team, we have an end to end strong technical understanding of Clinical SAS modules. Our expertiese includes CRF annotation, Creation of Specifications, Study Data Tabulation Model (SDTM) domain mapping , Analysis Data Model (ADaM) domain mapping, implementation of both SDTM and ADaM Reviewers guides, FDA Submissions using Pinnacle 21, CDISC control terms and so on. Our team of experienced personnel enables us to consistently map and deliver standard and quality datasets at a cost far more reasonable compared with other similiar service providers.      Our team is streamlined efficiently to design effective project management solutions and communicate it proactively to our clients and sponsors. This enables us to have a reliable level of consistency which in tern leads to achieving our defined milestones on time.