The Simplest Guide to Clinical Trials Data Analysis with SAS

This course offered by Course Plus will take you through the essentials of clinical trials data analysis using SAS software. It begins with an overview of the pharmaceutical industry and clinical trial phases, focusing on the types of data involved. Participants will dive into clinical study documents such as protocols, informed consent, statistical analysis plans (SAP), and case report forms (CRFs), providing a comprehensive understanding of clinical study documentation. The course then covers how to build clinical study reports (CSRs), emphasizing SAS programming steps, demographic data analysis, summary statistics, and the final report preparation. Real-world data processing examples and practical exercises ensure that students gain hands-on experience, enabling them to efficiently analyze clinical trial data in SAS.