Asia-Pacific Part II | Australia, New Zealand, India and Malaysia
This free webinar series on Medical Device Registration will cover the following topics on how to enter the market and meet regulatory compliance in Asia-Pacific (APAC) markets:
- Reasons to enter the medical device market in Australia, New Zealand, India and Malaysia.
- What does the regulatory approval process look like?
- How can you benefit from approval in Australia, New Zealand, India and Malaysia to enter other APAC countries?
- What are the main differences between the country-specific requirements and EU/US medical device regulations?
- What is the overlap and how can technical documentation efficiently be used in the roadmap?
- Latest updates on the regulatory developments in Australia, New Zealand, India and Malaysia.
Watch the webinar On-Demand.