FROKOST MED TERIAK

2. september 2026 kl 8.30-10.00

Knowing what you don’t know – leadership strategies for navigating complex industries 

Hanne Mette D Kristensen 

Biotech, medtech, and digital health companies compete on a global stage for both partnerships and investment. To succeed, they must meet high international industry standards from the outset. But what does that actually entail? And how can a newly established company with a promising idea ensure that all critical areas are adequately addressed? 

This meeting explores structured approaches to long-term business strategy development, helping companies build excellence across all essential domains — from scientific documentation, intellectual property rights (IPR), product and clinical development, to commercial execution and growth. 

How do I know I’m (not) a medical device?  

Tone Oftedahl Joakimsen 

Medical Device Regulations (MDR) have a significant impact on many digital health and medtech technologies currently under development. Importantly, even products that do not qualify as medical devices must be able to demonstrate and document their regulatory status. 

How can you determine whether your product is classified as a medical device? What documentation is required, and where should you begin? This seminar provides an introduction to regulatory classification, documentation requirements, and practical steps for navigating the regulatory landscape from the early stages of product development. 

Breakfast is served from 8.00 am. 

 Limited number of seats. 

Registration deadline: August 28th, 2026. 

Registration: Påmelding Frokost med Teriak