Level: Beginner
As of April 1, 2020, electronic data submission has been required for drug approval applications. This presentation will first introduce the CDISC data standards used in applications, followed by a demonstration of JMP Clinical , which excels in analyzing CDISC- compliant data.
He is a system engineer in the academic sales team of the JMP Japan division of SAS Institute Japan Co., Ltd. Previously, he worked in statistical analysis of clinical trials at a CRO and pharmaceutical company. He holds a Master of Science in Mathematics.
