Medical Device Registration in APAC and LATAM
In addition to the well-known regulatory markets in Europe and the United States, Qserve supports other emerging medical devices and IVD markets. With this Free Webinar Series on Medical Device Registration, our experts from around the globe will represent countries in the Asia-Pacific (APAC) and Latin-American (LATAM) markets and provide insights with experience from the field.
Regulatory pathways
The smartest way to access new medical device markets
Understanding the pros and cons of the various regulatory pathways for market access is essential to making informed choices to get a product to the market and knowing what is essential to ensure how to comply with all requirements.
Watch our On-Demand webinars to learn more about the regulatory framework in these countries. These webinars have been hosted in 2023 by our regulatory affairs associates.
Topics of the webinar series:
- Reasons to enter the medical device market in the specific country
- What does the regulatory process look like?
- How can you benefit from approval to enter other APAC or LATAM 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 the countries.
Asia-Pacific Part 1 | China and Singapore
How to enter the APAC markets and meet regulatory compliance in China and Singapore.
On-Demand Recording
Asia-Pacific Part 2 | Australia, New Zealand, India, Malaysia
How to enter the APAC markets and meet regulatory compliance in Australia, New Zealand, India and Malaysia.
On-Demand Recording
Latin-America Part 1 | Brazil and Mexico
How to enter the LATAM markets and meet regulatory compliance in Brazil and Mexico.
On-Demand Recording
Latin-America Part 2 | Colombia and Argentina
How to enter the LATAM markets and meet regulatory compliance in Colombia and Argentina.
On-Demand Recording
Global Market Access
Benefit from our worldwide regulatory proficiency and tap into local expertise across the globe. We possess a comprehensive understanding of national regulations and their intersections. Starting from the initial concept to achieving global market access, we're dedicated to crafting your global strategy.
Market Access
Medical Device Registration Support
Do you need assistance with your regulatory strategy and medical device registration? Qserve is your trusted partner for worldwide market access. Together, we can chart a course towards the best strategy and a roadmap that delivers results.
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