Level: Beginner
【Presenter】
Hideaki Miyata, JMP Japan Division, SAS Institute Japan Co., Ltd.
[Announcement summary]
2020 Four Moon 1 From day to day, the submission of electronic data has been required for drug approval applications. In this lecture, first of all, it will be used for application CDISC Introducing data standards. after that, CDISC Has strengths in analyzing compliant data JMP Clinical Will be introduced with a demo.
[Presenter Profile]
SAS Institute Japan Co., Ltd. JMP In the academic sales team of the Japan Division SE In charge of. In my previous job CRO Engaged in statistical analysis of clinical trials at a pharmaceutical company. Master of Science (Mathematics).
