Over 20 years of expertise
Yosuke Kimura has over 20 years of expertise in Research and Development, Regulatory Affairs within the Pharmaceutical Industry.
At Medicago he holds the important role of overseeing all aspects of late-stage clinical developments, including clinical operations, clinical safety and pharmacovigilance, regulatory affairs, quality assurance and quality control.
Prior joining Medicago in 2021, Yosuke was Vice President, Head of Global Regulatory Affairs Department at Mitsubishi Tanabe Pharma Corporation (MTPC). In that role, Yosuke was responsible for the development of Japanese domestic products and post-marketing and commercial regulatory activities and for the development of regulatory strategies to expand the development of products to Europe, U.S. and Asia and to obtain approvals from regulatory authorities globally.
Yosuke holds a Ph.D. in Science and Technology from Kobe University and always has been passionate and driven by science.