Significant changes in Japanese pharmaceutical regulations and procedures are impacting the development of new drugs in Japan as well as global development programs. This short course will describe the major drivers of the regulatory system, including the Pharmaceuticals and Medical Devices Agency (PMDA) and Ministry of Health, Labor and Welfare (MHLW), regulatory procedures during drug development (consultations with PMDA and clinical trial notifications), the integration of Japanese drug development with East Asian and global drug development, orphan drug regulation, and J-NDA preparation and review. Several development strategies available to address Japanese requirements for new drug approval, as well as selected post-approval requirements, will be discussed.
Need approval in order to attend?
Download and fill out our Justification Letter to demonstrate to your supervisor why this is a must-attend event.
Enhance your experience and register for two or more short courses at the same time and receive $50 in savings.
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Upon completion of registration, participants will gain access to the following:
- Live Event Access
- Presentation Slides
- Access to recorded sessions, on demand for 4 months post event
Who should attend?
- Explain the major elements of the Japanese regulatory system
- Describe the regulatory procedures during development, registration, and post-approval
- Discuss specific attributes of the Japanese regulatory system and their impact on local and global development strategies.