NXTGEN Hightech Biomedical and High Tech NL invite you to join an insightful webinar on September 4, 2024, from 16:00 to 17:00 CET. This engaging and practical webinar will feature hands-on advice drawn from the extensive experience of QServe, a leading consultancy in regulatory affairs. Attendees will gain valuable insights into: The importance of early regulatory involvement
Essential milestones necessary for preparing the launch of your biomedical innovations.

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Who Should Attend?

This webinar is designed for professionals in the fields of Biomedical Engineering, Applications, and Life Sciences who are keen to navigate the complex regulatory landscape and successfully bring their innovations to market.

Register on time because there are limited spots available for this webinar.

Programme

Welcome by Edwin Roovers, High Tech NL Life Science

How to bring your idea to the market

• Which is the first country I want to market my device?
• Classification > Do I have a device?
• High level overview IVDR, MDR, FDA
• Manufacturing & responsibilities
• Choosing suppliers, subcontractors and OEM’s

Case study lab-on-chip

• Early phases what’s important
• What is worth investigating
• Common mistakes
• Time vs cost
• Exit strategy