OVERVIEW
FOCUS AREAS
More than 25 years of experience in research and development in the pharmaceutical industry.
Regulatory Science in Japan
Oncology
Emiko Takezawa has over 25 years experience working in Global pharmaceutical companies.
She has mainly been involved in the development of oncology drugs as regulatory lead and contributed to obtaining multiple approvals in Japan.
She has extensive experience in regulatory affairs, with expertise in global regulatory strategies and the integration of Japan into global product development programs, specifically in the oncology area.
-
EDUCATION:
- Bachelor of Pharmaceutical Sciences, Chiba University
- Master of Pharmaceutical Sciences, Chiba University
CERTIFICATIONS:
- Pharmacist
Ready for Regulatory Clarity?
Stay informed as the regulatory landscape evolves.
Subscribe to our blog to receive the latest updates on policy changes, FDA developments, and their impact on the life sciences industry.