Clinical SAS
Clinical SAS is a specialized application of the Statistical Analysis System (SAS) designed for managing, analyzing, and reporting clinical trial data. It ensures data accuracy, reliability, and compliance with international standards such as FDA, CDISC, and ICH. By transforming raw clinical data into structured, meaningful insights, Clinical SAS supports effective decision-making in clinical research. It plays a crucial role in generating accurate statistical outputs, ensuring smooth regulatory submissions, and maintaining data integrity throughout the study lifecycle.
At UNIFIED POINTS TECH, we leverage Clinical SAS to provide high-quality, submission-ready datasets and analytical reports that meet global compliance standards. Our expert team combines advanced programming, data analysis, and statistical modeling to ensure robust and reliable results. We assist pharmaceutical, biotechnology, and CRO organizations in achieving faster regulatory approvals through efficient data processing and validation. With our Clinical SAS expertise, we help clients streamline their research operations, enhance data transparency, and ensure successful study outcomes.
CDISC Standards Implementation (SDTM & ADaM)
CDISC Standards Implementation (SDTM & ADaM) is a crucial part of clinical data management that ensures consistency, transparency, and compliance across all study datasets. At UNIFIED POINTS TECH, we specialize in transforming raw clinical data into standardized formats using SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) structures. These standards are designed to improve data organization, making it easier for sponsors and regulatory authorities to review, analyze, and interpret results efficiently. By implementing CDISC standards, we help clients meet the stringent requirements of global regulatory bodies such as the FDA and EMA.
Our expert team at UNIFIED POINTS TECH ensures complete data traceability from collection through submission by applying precise mapping and validation techniques. We follow best practices to create compliant, well-documented datasets that facilitate faster reviews and minimize the risk of regulatory rejections. Through our structured approach, we enhance the quality, consistency, and reliability of clinical data. This allows our clients to achieve smoother submission processes, improved efficiency, and higher confidence in their clinical research outcomes.
SAS Programming and Data Analysis
SAS Programming and Data Analysis form the foundation of efficient and compliant clinical data management. At UNIFIED POINTS TECH, we design and execute robust SAS programs that handle data cleaning, transformation, and statistical analysis with precision. Our systematic approach ensures that raw clinical data is transformed into accurate, well-structured datasets ready for statistical evaluation. We focus on maintaining data integrity and compliance with global regulatory standards throughout the process. This enables sponsors to make reliable, data-driven decisions in their clinical research.
Our team of experienced SAS programmers at UNIFIED POINTS TECH ensures that every dataset and output is submission-ready and aligned with FDA and CDISC requirements. We use validated programming techniques to generate precise statistical analyses that support clinical study findings and regulatory documentation. By integrating automation and quality control, we minimize errors and improve efficiency. Our goal is to deliver high-quality analytical outputs that enhance the credibility of clinical results and accelerate successful regulatory submissions.
