Data harmonization in clinical research studies: Challenges and opportunties

Data harmonization is crucial in multi-site clinical trials to ensure data integrity, comparability, and usability. In this video, we discuss the importance of data harmonization, outlining key challenges and best practices to help teams unlock data's full potential for advancing medical research.
Data harmonization in clinical research studies: Challenges and opportunties
Video blog post by Rym Ben Othman

Data harmonization plays a pivotal role in ensuring the integrity, comparability, and usability of the collected data. Effective data harmonization is essential for drawing meaningful conclusions, supporting regulatory submissions, and advancing medical research. However, achieving seamless data harmonization across multiple sites presents complex challenges that clinical research teams must carefully navigate. The path to harmonized data is laden with obstacles, from disparate data collection methods to inconsistent terminologies and varying quality control measures.

This short video highlighted the importance of data harmonization in multi-site clinical trials. We provided an overview of the key challenges and best practices to help researchers and data managers successfully navigate this critical process. By understanding the intricacies involved and implementing robust strategies, clinical trial teams can unlock the full potential of their data and drive innovation.

About the author
Rym Ben Othman

Rym Ben Othman

Co-founder and Chief Scientific Officer at RAN BioLinks, Rym brings over 20 years of experience leading sizeable clinical research projects in academia and Industry

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