Do you want to take your digital health and medical device ideas to a European market? The Regulatory Pathways to Market Bootcamp supports early-stage start-ups to ease their entry into market.
In this 10-week online programme you will understand the highly regulated pathway within the European healthcare system and identify potential pathways to reimbursement. With the support of industry experts, you will design a go-to-market path for your start-up.
Applications to the Regulatory Pathways to Market Bootcamp are currently closed. Be the first to know about upcoming programmes and opportunities that may be a good fit for you by joining our mailing list.
Attend practical workshops and case studies covering each process applicable to device development and marketing
Get deep understanding of regulatory strategies, life cycle management and pathways to reimbursement
Receive the tools and knowledge to develop a complete go-to-market strategy for your start-up
Tap into the EIT Health network of 140+ partners to increase the visibility of your start-up
Access the EIT Health Alumni community to meet like-minded entrepreneurs and access the suite of EIT Health programmes
Don’t miss the deadline! Sign up using the EIT Health application portal, create a log-in and start your application
Be part of one of the 10 teams to get selected and enter the programme
Receive training on medical devices regulation, in-vitro diagnostic medical devices regulation, reimbursement strategies and health technology assessment
Alongside our experts and with your new knowledge, you’ll design your own start-up’s go-to-market strategy
We’re looking for start-ups or SMEs that:
There is a commitment fee of €350 per company once accepted in the programme
Take a look into the programme’s info session, where the Regulatory Pathways to Market Bootcamp’s manager presents the programme into more detail and answer live questions.
Applications to Bridgehead are currently closed. If you are interested in this programme register to our newsletter to receive similar opportunities.
Sign up for updates
Project Manager, Instituto Pedro Nunes
Medical Devices and In Vitro Diagnostics Regulation Expert, Instituto Pedro Nunes
Project Management, Medical Valley EMN
Health Economist, Syreon Research Institute
INNOVA-Integrated Health Solutions, Medtronic Ibérica
INNOVA-Integrated Health Solutions, Medtronic Portugal
Project Manager, Complear
Regulatory Affairs Expert, Complear
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