Medidata announced that the Medical Research Collaborating Center has selected Medidata Rave to accelerate the overall regulatory data submission process during clinical trials. MRCC, which is under the Biomedical Research Institute of Seoul National University Hospital (SNUH), will leverage the Medidata Clinical Cloud to facilitate clinical trials with its partner pharmaceutical companies. MRCC was established as a division in the Department of Education and Research for SNUH, serving as a coordinating center for large scale multicenter clinical trials and epidemiologic studies. By integrating Medidata Rave, the world’s leading solution for capturing, managing and reporting patient data, and complying with international standards such as CDISC1, MRCC aims to further standardize data management and statistical analytics to meet global standards and regulatory submissions, including those by the FDA. Electronic data management systems that comply with global regulatory standards are necessary for new drug submissions. With Medidata Rave, MRCC expects to improve the process of data management and plans to make a transition from Clinical Data Acquisition Standards Harmonization (CDASH) to Study Data Tabulation Model (SDTM).