PrintJapan has the second largest medical device market in the world. How you determine whether product registration makes sense is largely a function of the device reimbursement. All too often, a medical device company will go through the regulatory hurdles and long approval times in Japan to then realize that they have not determined if their pricing strategy will work. This webcast will explain the reimbursement process, including reimbursement strategies as well as what key documents and information is necessary to submit to the PMDA. It will also explain the approximate timeframes for different reimbursement schemes. This 90-minute session will include a 60-minute presentation, followed by 30 minutes of Q&A.
- Japan healthcare overview
- Overview of Japan's reimbursement system
- Payment system
- Functional Category
- Fee-For-Service
- Reimbursement categories for medical devices
- Examples of each reimbursement category
- A1
- A2
- B
- C1
- C2
- F
- Determining appropriate reimbursement category
- Detailed application forms for some reimbursement categories
- Application and review process, timeframes
- Examples of each reimbursement category
- How reimbursement rates are set
- How to get the maximum reimbursement for your device
- The key documents to get product reimbursement
- How to fill out the key documents
- Tips for success
- How reimbursement prices are adjusted
- Reasonable Zone (R-Zone)
- Foreign Average Reference Price (FRP)
- New trends in the reimbursement system in Japan