Understanding and navigating the European regulatory landscape is a crucial step for those working in the medical device and digital health sectors. To support this journey, applications are now open until 28 May for the EIT Health Regulatory Pathways to Market Bootcamp 2025, a structured 12-week training programme designed to provide in-depth knowledge and practical tools for regulatory compliance and market access.
Over the past two editions, the Bootcamp welcomed over 60 participants from 30 companies across Europe, resulting in several success stories — including 4 companies that have managed to attract €3.6M of investment following their participation.
The programme offers comprehensive support in key areas such as:
● Development of a complete regulatory strategy
● Health Technology Assessment (HTA) and market entry analysis
● Reimbursement opportunities and regulatory pathways
● Implementation of regulatory requirements from the early development stage
The Bootcamp is open to professionals, startups, organisations, and stakeholders involved in regulatory affairs, technology assessment, and market access strategies for medical devices and in vitro diagnostic medical devices. The participation fee is 1,000 euros, with a 50 percent discount for the top 10 ranked applicants in the selection process.
