Insight into Requirements of PMDA for Marketing Medical Products in Japan 2017 is a webinar that covers topics such as:
- Why make an entry into this key market for your medical devices?
- A brief overview of the importance of the Japanese Market
- Determining the regulatory process for your device and the classification scheme
- Introduction to its healthcare system and regulatory requirements
- Basic compliance requirements of MHLW Ordinance #169
- The heavy responsibilities of the Marketing Authorization Holder(MAH)
- Submission pathway and completion to obtain the PMDA Certification to distribute your device in Japan
Insight into Requirements of PMDA for Marketing Medical Products in Japan 2017 is intended for attendees from medical device companies:
- Business Managers
- Regulatory Managers and Associates
- Business Analysts
- Quality professionals who want to know about PMDA requirements for medical devices
- Strategic planners in the medical device industry at all levels
- Small and large fast growing medical device manufacturers
