ContactMeet the Experts Empowering Your MedTech Success
At IGES MedTech, we actively engage with the global MedTech community through industry-leading events and exclusive webinars. These occasions provide a unique opportunity to connect with our experts, gain actionable insights, and discuss how we can support your journey to market success.
Whether you're attending an international conference or joining one of our webinars, our team is ready to share expertise and explore tailored strategies to help your medical device succeed in today's competitive healthcare landscape.
Below, you'll find details of our upcoming events and webinars. Let's meet and work together to bring innovative solutions to patients worldwide.
Join Our Upcoming Webinars at IGES MedTech
Tuesday, 06.05.2025
Online
Mattias Kyhlstedt, Michel Verhasselt, Michael Weisser
Webinar
EU HTA for Medical Devices and IVD’s
HTA (Health Technology Assessment) has long been used to evaluate certain medical devices and diagnostics. Now, a new EU HTA regulation is on the horizon, and it’s poised to bring major changes for the products it covers.
This webinar is the first in a series exploring how the new EU HTA regulation might influence the MedTech and IVD industries. Even though many details of the regulation are still being finalized, we’ll share our perspective based on what we know so far and our experience in the field.
In this session, we’ll cover:
- The history and current role of HTA in the medical device and diagnostics sector.
- Insights from EUnetHTA and what they mean for the future.
-Which products are eligible for EU HTA?
- An overview of the EU HTA process and how it works.
- Anticipated impacts in different countries – what to expect across Europe.
- A deep dive into how the EU HTA process might link to national decision-making, with a focus on:
- Germany
- France
- Recommended actions to help you prepare for these changes.
Meet the IGES MedTech Team at Leading Industry Events
Tuesday, 06.05.2025
Online
Mattias Kyhlstedt, Michel Verhasselt, Michael Weisser
Webinar
EU HTA for Medical Devices and IVD’s
HTA (Health Technology Assessment) has long been used to evaluate certain medical devices and diagnostics. Now, a new EU HTA regulation is on the horizon, and it’s poised to bring major changes for the products it covers.
This webinar is the first in a series exploring how the new EU HTA regulation might influence the MedTech and IVD industries. Even though many details of the regulation are still being finalized, we’ll share our perspective based on what we know so far and our experience in the field.
In this session, we’ll cover:
- The history and current role of HTA in the medical device and diagnostics sector.
- Insights from EUnetHTA and what they mean for the future.
-Which products are eligible for EU HTA?
- An overview of the EU HTA process and how it works.
- Anticipated impacts in different countries – what to expect across Europe.
- A deep dive into how the EU HTA process might link to national decision-making, with a focus on:
- Germany
- France
- Recommended actions to help you prepare for these changes.
