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This presentation provides an overview
of Taiwan's medical device regulations as well as discusses
the most recent regulatory issues. This presentation
is from Pacific Bridge Medical's Taiwanese webcast on April 20,
2006. This presentation has 70 slides. The speaker is PBM's partner
in Taiwan.
Click
here to see a sample page of our webcast presentation.
The following topics are covered
in this presentation:
- Overview of Taiwan's
healthcare system
- Recent Department of
Health changes
- Product registration
requirements
- New medical device
regulations
- Product reimbursement
/ Price list
- Good Manufacturing
Practice (GMP)
- Quality System Documentation
(QSD)
- Good Clinical Practice (GCP)
- Local clinical trials
- Post-marketing surveillance
- Third party registration
- How to expedite the
registration process
This presentation
is designed for medical device professionals in regulatory
affairs, business development, international sales and
marketing, and anyone who wants to be current on a number
of Taiwan's new regulatory issues.
Click here to purchase a hard
copy of the PowerPoint
presentation.
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