BACKGROUND
FOCUS AREAS
Naoya Kato joined ELIQUENT Japan in 2008, following a distinguished career of global drug development experience.
Regulatory management of the global strategy integrating Japan into global product development.
Naoya Kato joined IDEC (now ELIQUENT Japan, Inc.) in 2008, following a distinguished career of global drug development experience.
Mr. Kato has more than 30 years experience working with large multi-national pharmaceutical companies.
He has broad experience in global drug development with particular expertise in the clinical and regulatory management of the global regulatory strategy integrating Japan into global product development programs.
With his broad experience in the regulatory science for the development of global product development strategies, he achieved several successful globally integrated programs involving Japan by leading global project teams. He has contributed to the clients’ successful attainment of marketing approvals ahead of schedule. Leveraging his extensive skills and experience, the clients have overcome various obstacles and, in some cases, obtained marketing approvals simultaneously in Japan, the US, and Europe.
-
EDUCATION:
- Master of Science from Meiji Pharmaceutical University Graduate School in Pharmacological Science
- B.A. from Meiji Pharmaceutical University in Pharmacy
-
PROFESSIONAL EXPERIENCE:
Achieved several successful globally integrated programs involving Japan by leading global project teams through PMDA consultations and clarifying the regulatory requirements for Japanese submissions for global product development programs:
- Global Product Development Strategies Management
- Japan Product Development Management
Regulatory & Medical Writing Solutions
Experience the power of clarity
From streamlining regulatory approvals to enhancing market presence, our medical writing solutions support your regulatory objectives and strengthen your market position.