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!

Apply now

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

Applications

15 January to 28 May

Evaluation

16 – 20 June

Invitation for interviews

23 June

Interview

1, 8 and 15 July

Inform of acceptance

22 July

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 now

Meet 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

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Stay up to date about upcoming programmes and opportunities that may be a good fit for you

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Regulatory Pathways to Market Bootcamp

What you get

HANDS-ON EXPERIENCE

REGULATORY MASTERY

PERSONALISED PLAN

NETWORKING OPPORTUNITIES

ALUMNI SUPPORT

CERTIFICATION

How it works

1. APPLY

2. GET SELECTED

3. LEARN

4. DESIGN

Dates of the process

Applications

Evaluation

Invitation for interviews

Interview

Inform of acceptance

Who should apply?

Info Session

Ready to apply?

Meet the team

Maria Cravo

Ana Brito

Jonas Friedrich

Kristóf Gyongyosi

Jorge Posada

Célia Cruz

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

HANDS-ON
EXPERIENCE