Regulatory Pathways to Market Bootcamp
Are you an early-stage start-up with an evolutionary idea for a digital health or medical device? Then the Regulatory Pathways to Market Bootcamp is for you.
This tailored Bootcamp provides you with specialised assistance to guide you through the highly regulated pathway of the European healthcare system whilst streamlining your innovation’s entry to the market.
Embark on this transformative 12-week online journey alongside industry experts, kicking off on 8 September and concluding on 28 November 2025. You’ll be assisted with insights crucial for identifying reimbursement routes, as well as expert guidance to craft a custom market strategy for your start-up to thrive.
Applications to Regulatory Pathways to Market Bootcamp are now open. Don’t miss your chance and be a part of this journey. Apply by 28 May!
What you get
HANDS-ON
EXPERIENCE
Apply your learning to the real world – gain practical expertise through workshops and case studies
REGULATORY MASTERY
Gain a deep understanding of EU regulations for taking digital medical devices to market
PERSONALISED PLAN
Receive expert guidance to develop a go-to-market strategy specifically for your start-up
NETWORKING OPPORTUNITIES
Tap into the EIT Health network of over 140 partners to increase the visibility of your start-up
ALUMNI SUPPORT
Join EIT Health’s alumni network to collaborate with other entrepreneurs and access further training
CERTIFICATION
Get an attendance certificate if you successfully complete the Bootcamp’s Quiz
How it works
1. APPLY
Apply from 15 January to 28 May. Sign up using the EIT Health portal and start your application
2. GET SELECTED
Secure your spot among the top 20 teams to enter the programme
3. LEARN
Master medical device regulation, reimbursement strategies and health technology assessment
4. DESIGN
With your new knowledge, work with our industry experts to craft your go-to-market strategy
Dates of the process
Curriculum
Who should apply?
Ready to catapult your innovation into the heart of the European market?
We’d like to hear from you if you are a start-up or SME that:
- Is incorporated in a Horizon Europe country
- Are TRL 3-6
- Has experience with the technology and knowledge in HealthTech
Please note:
- Once accepted into the Bootcamp there is a commitment fee of €1.000,00. We will give a 50% discount to the top 10 companies classified according to their scores.
- The market value of this programme is €6.000,00. With EIT Health support, discounts are applied.
- Each company will have access to training for 2 participants.
- VAT will be added if applicable according to EU legislation.
"The Bootcamp's structure and content impressed us greatly, providing essential knowledge and tools for regulatory compliance in our medical device sector. It guided us through compliance stages, emphasizing Quality Management Systems and Risk Management. With expert support, it broadened our perspective on factors like regulatory obligations, timelines, and cost implications for our go-to-market strategy."
Bootcamp Participant
2023 Edition
"The EIT Health Regulatory Pathways to Market Bootcamp was very helpful for us to finetune our regulatory strategy."
Bootcamp Participant
2023 Edition
"This bootcamp was great to get a comprehensive understanding of the highly regulated pathway within the European healthcare system, to give us experience in health technology assessment and gain hands-on experience in market access."
Bootcamp Participant
2023 Edition
Info Session
Webinars are a great way to find out if the programme is a right fit for you. Take a look at the webinar recording that took place in March 2025.
Watch recording.
Ready to apply?
Applications to Regulatory Pathways to Market Bootcamp are now open. Don’t miss your chance and be a part of this journey. Apply by 28 May!
Apply nowMeet the team
Maria Cravo
Programme Manager
Ana Brito
Head of Medical Devices Unit, Instituto Pedro Nunes
Jonas Friedrich
Project Management, Medical Valley EMN
Kristóf Gyongyosi
Project Management, Syreon Research Institute
Jorge Posada
INNOVA-Integrated Health Solutions, Medtronic Ibérica
Célia Cruz
Regulatory Affairs Expert, Complear
Partners
Instituto Pedro Nunes
Medical Valley EMN e.V
Syreon Research Institute
Medtronic Iberica S.A
Medtronic Portugal LDA
Complear
Sign up to our newsletter
By joining our mailing list you will:
- Be the first to know when this programme is open for applications
- Stay up to date about upcoming programmes and opportunities that may be a good fit for you