Join the Clymb Clinical Team for a Hands-On ARS Training

Clymb Clinical is hosting an in-person CDISC ARS Hands-On Implementation Training at our headquarters in Burlington, MA. This hands-on implementation training will provide an in-depth overview of the ARS model and practical examples illustrating the implementation of the model using common safety displays.

Training Agenda

This training consists of:

• ARS v1.0 project overview including business cases.
• A description of artifacts included in ARS v1.0.
• A detailed review of the main components of the ARS v1.0 model and how they are used to define analyses and outputs.
• Exercises to help reinforce attendees’ understanding of the main components of the model.
• Discussion of the components of the ARS v1.0 model that support production of ARM for Define-XML.
• Discussion and example of how ARS v1.0 can support the implementation of the FDA Standard Safety Tables and Figures Integrated Guide
• A review of ARS v1.0 implementations including a demonstration of the automation of analysis through use of ARS metadata.
• Exercises that allow attendees to create ARS metadata using the TFL Designer.
• Overview of the upcoming eTFL portal and associated assets.

Learning Outcomes

At the end of this course, learners will be able to:

• Explain how ARS facilitates automation and regulatory compliance in analysis reporting
• Describe the CDISC Analysis Results Standard (ARS) model and its key components
• Apply the ARS model to define and structure analysis results
• Utilize the TFL Designer tool to create ARS metadata

Register now

Secure your spot and gain hands-on experience with CDISC ARS implementation.

Register Here: CDISC – ARS Hands-On Implementation Training (In-Person | Boston, Mass | 11 April 2025)