Clinical Data Management (CDM) is a pivotal element in clinical research trials, focusing on the collection, integration, and validation of data obtained from research studies. Its primary goal is to ensure that data from clinical trials is accurate, complete, and maintained in a secure and confidential manner. CDM involves the use of rigorous protocols and sophisticated software systems to streamline the data collection process, minimise errors, and ensure that the data is reliable and ready for analysis. This process supports the integrity of the trial and the validity of the results, facilitating a smooth transition from data collection to statistical analysis and, ultimately, to the interpretation of findings. By ensuring high-quality data management practices, CDM plays a vital role in advancing medical research, aiding in the development of new treatments, and contributing to evidence-based medicine.