How to get regulatory approval faster and cheaper

How to get regulatory approval faster and cheaper

Wednesday May 6, 2026 10:20 - 10:40 Innovation Area

Track: Innovation area

If you are building a health tech product and plan to sell it to professional healthcare, most products need to be regulatory approved. This is very costly, takes a long time and huge effort. It is also really difficult to understand where to start, and how to run the process.

Jesper Grønbæk, CEO & Founder of Health Tech Hub Copenhagen, will based on 7 years working with start-ups within health tech, having helped more than 100 start-ups and scaleups, share their learnings around this area.

How can you avoid being regulated in the EU?

How can you get to the lowest level of regulation in the EU?

How do you start your regulation journey? What can you expect? How do you build the right culture? Which tools to use? Which consultants to use? How do you choose the right Notified Body? How can you get your MDR regulation as fast as possible?

These will be some of the questions, Jesper, will share insights into in his presentation.

Health Tech Hub Copenhagen, is a non-profit organisation, that has spent the last 7 years helping health tech startups succeed, and the last 2 years really understanding how we in Europe, can help startups get their product faster to market with the necessary regulatory tools.

Language

English

Topic

Technology

Seminar type

Live + On site

Lecture type

Extended 55 min

Objective of lecture

Tools for implementation

Level of knowledge

Introductory

Target audience

Management/decision makers
Organizational development
Technicians/IT/Developers
Researchers
Students

Keyword

Actual examples (good/bad)
Management
Innovation/research
Documentation
Apps
Law, Judicial procedures
Patient safety
Information security
Government information

Conference

Vitalis

Lecturers

Jesper Grønbæk Lecturer

Health Tech Hub Copenhagen

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