Recordings, The Hyve Events

From research to regulators: effectively using SDTM & OMOP

Everything you should know about Data SDTM and OMOP

08 December, 2025

Speakers

Berber Snoeijer

Manager Innovative Process and Solution Design @ ClinLine

Julia Kurps, PhD

Consultant specialized in OHDSI and RADAR-base @ The Hyve

Architha Keijsers, PhD

Biomedical Research Business Analyst @ The Hyve

High-quality data is essential for generating real-world insights and reliable clinical research. This webinar explores the best practices for data quality assurance using OMOP Common Data Model and explores how the OHDSI community tackles these sources.

We will provide a technical look at how integrating tools like the Data Quality Dashboard (DQD) and Achilles into ETL pipelines can systematically check your data to determine whether or not your observational data is fit for large-scale analytics. Our goal is to enhance the reproducibility of real-world data and provide you with strategies to strengthen your ETL process and data pipelines.

This session is for data engineers, data scientists, and ETL developers responsible for managing observational health data and ensuring its integrity for analysis. 

This webinar covers

OMOP, The Hyve and ClinLine Introduction

Overview of real-world data (RWD) and its role in regulatory processes

Comparison of the OMOP Common Data Model (CDM) and the clinical trial data standard SDTM

Using OMOP as a repository and managing mappings from SDTM to OMOP and OMOP to SDTM

European flagship projects illustrating practical applications, including DARWIN EU, GREG, and EHDEN

Summary of the use of RWD for regulatory processes

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