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Clinical SAS with CDISC, SDTM and ADAM

Date:- 23th June 2023

Timing:- 2:00 PM

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Instructor: Ram V

Language: English, Hindi

Enrolled Learners: 1038

Validity Period: Lifetime

Join us for a free webinar that provides an introduction to the powerful combination of Clinical SAS with CDISC standards, specifically SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model).

In the ever-evolving landscape of clinical research, adherence to standardized data representation and analysis methodologies is essential for efficient data management, interoperability, and regulatory compliance. This webinar will delve into the fundamental concepts and practical implementation of Clinical SAS with CDISC standards, enabling attendees to harness the full potential of SAS software for clinical trial data management and analysis.

Key topics to be covered in this webinar include:

  1. Overview of Clinical SAS: Gain insights into the capabilities and features of SAS software for data management, statistical analysis, and reporting in the clinical research domain.
  2. Introduction to CDISC Standards: Understand the role and importance of CDISC in establishing global data standards for clinical research data interchange and integration.
  3. SDTM Essentials: Learn the basics of SDTM and its role in standardizing the organization and presentation of clinical trial data. Explore the SDTM domain structure and key concepts for mapping and transformation.
  4. ADaM Implementation: Explore the principles and guidelines of ADaM for creating analysis-ready datasets to support statistical analyses. Discover how to structure data for efficacy and safety assessments using ADaM standards.
  5. Data Transformation and Mapping: Gain practical insights into the process of transforming raw clinical trial data into CDISC-compliant formats, including mapping variables to SDTM and ADaM domains.
  6. Statistical Analysis with SAS: Discover how to leverage SAS software to perform statistical analyses on SDTM and ADaM datasets. Learn about SAS procedures and programming techniques for generating summary statistics, performing statistical tests, and producing analysis reports.
  7. Reporting and Regulatory Submissions: Understand the importance of generating accurate and compliant outputs for clinical study reports and regulatory submissions. Learn how to create tables, listings, and figures (TLFs) using SAS for effective data presentation.

Whether you are a clinical data manager, biostatistician, clinical programmer, or a professional working with clinical trial data, this webinar offers valuable insights into the integration of Clinical SAS with CDISC, SDTM, and ADaM. Join us to enhance your understanding of standardized data management and analysis practices, ultimately streamlining your clinical research workflows.

Don't miss this opportunity to explore the synergy between Clinical SAS and CDISC standards. Reserve your spot now for this free webinar on Clinical SAS with CDISC, SDTM, and ADaM!


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