Principal Reviewer
Pharmaceuticals and Medical Devices Agency
Chiyoda-ku, Tokyo, Japan
Dr. Murakami joined Pharmaceuticals and Medical Devices Agency (PMDA) Japan as medical device reviewer in 2005. She's been involved in international regulatory harmonization activities such as GHTF/IMDRF MC and WGs, Japan-US Harmonization by Doing (HBD), ISO TC194 and TC210, Harmonization by Doing (HBD), etc for more than 15 years. After working as medical device QMS auditor in PMDA and as deputy director at Ministry of Health, Labour and Welfare for several years, now she works as Principal Reviewr for Office of Software as a Medical Device in PMDA.
Disclosure(s): No financial relationships to disclose
Monday, March 11, 2024
8:10 AM – 9:10 AM ET
Monday, March 11, 2024
8:10 AM – 8:20 AM ET
Monday, March 11, 2024
8:50 AM – 9:10 AM ET