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 10-week online journey alongside industry experts. 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.

Ready to launch your groundbreaking digital health or medical device? Secure your spot now!

Apply here

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

How it works

1. APPLY

Don’t miss the deadline! Apply by 21 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

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 a team of two to five people
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.
Only 2 members per team can participate in the mentoring sessions.
VAT will be added if aplicable according to EU legislation.

Info Session

Tune in to our upcoming informational webinar! Join us as the programme team unveils its benefits and listen firsthand to a past participant’s Bootcamp journey.

Join the webinar on 23 April at 12 PM CET.

Ready to apply?

Click below and complete the application to get a chance to secure your spot on this entrepreneurial journey. All you have to do is, register on our platform, verify your account, and select the application form for Regulatory Pathways to Market Bootcamp.

Apply now

"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

Meet the team

Natália Lescura

Project Managment, Instituto Pedro Nunes

Sandra Balseiro

Medical Devices and In Vitro Diagnostics Regulation Expert, 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

Inês Matias

INNOVA-Integrated Health Solutions, Medtronic Portugal

Carla Santos

Project Manager, Complear

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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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

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SEARCH OUR SITE

Regulatory Pathways to Market Bootcamp

What you get

HANDS-ON EXPERIENCE

REGULATORY MASTERY

PERSONALISED PLAN

NETWORKING OPPORTUNITIES

ALUMNI SUPPORT

How it works

1. APPLY

2. GET SELECTED

3. LEARN

4. DESIGN

Who should apply?

Info Session

Ready to apply?

Meet the team

Natália Lescura

Sandra Balseiro

Jonas Friedrich

Kristóf Gyongyosi

Jorge Posada

Inês Matias

Carla Santos

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

ALUMNI
SUPPORT