Overview

Faced with a challenge in SDTM data validation, SGS sought an innovative solution to replace the traditional method of SDTM double programming in clinical database setup. How could we start SDTM database creation before real clinical study data was available? Solving this conundrum became crucial in complex studies with safety meetings shortly after FPI, numerous protocol amendments and eCRF mid-study updates, which demanded constant rapid and compliant SDTM data delivery. 

In this webinar, we will showcase the unique validation methodology SGS developed, that eliminates the need for double programming and ensures an efficient setup phase to save valuable time.

Let us tell you why you should attend:

• Discover a clever way to save valuable time, especially when swift SDTM data delivery is essential.
• Explore a unique approach to fast SDTM data adjustments
• Learn how our innovative method - starting programming prior to real study data - guarantees 100% validation 
• Understand why technical expertise is no longer a bottleneck, due to our approach simplifying the process.
• Gain insights from practical examples showcasing successful dummy data conversion into SDTM-compliant datasets.

Agenda

• Exploring SGS's distinctive approach
• Practical examples showing key validation learnings
• Q&A session: engage with experts, clarify your doubts

Target Audience: The webinar is aimed at all clinical research professionals involved in data management, data programming, data technology and process improvements. 

Language: English

Can't make a live session? Register now to automatically receive a complimentary recording after the live event. 

For further information, please contact: clincalresearch@sgs.com

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