PATH Bootcamp
PROJECT DETAILS
The Pathways for Regulatory and Market Access Bootcamp (PATH Bootcamp) is a 13-week training program designed to introduce participants to the complex European regulatory landscape for Medical Devices (MDs) and In Vitro Diagnostic Medical Devices (IVDs).
The program combines live sessions, recorded content, Q&A sessions and practical exercises, and is structured around three core modules:
- Introduction to Regulatory Compliance
- Basics in early Health Technology Assessment (eHTA)
- Introduction to Market Access and Reimbursement Strategies
This training is delivered in an e-learning format combining a learning platform and live sessions via Zoom.
- Course period: 14 September to 11 December 2026
- Total workload: 69 hours (24 hours of synchronous sessions and 45 hours of asynchronous learning)
The course is delivered in English.
For the full program agenda, please consult: here
The recruitment period (registration and payment) is open until 14 August 2026.
Two registration options are available:
- Course only
- €600* per individual participant
- €1,000* per team (2 participants)
- Course + 8 hours of mentoring
- €1,400* per individual participant
- €1,800* per team (2 participants)
Note: For team registrations (2 participants), the mentoring package includes a total of 8 hours per team (not per participant).
- €1,400* per individual participant
Women in HealthTech Campaign
Available for women individual participants with registration and payment completed between 26 June and 31 July 2026:
- Course only: €500* per individual participant
- Course + 8 hours of mentoring: €1,300* per individual participant
*VAT will be added if applicable according to EU legislation
Ready to accelerate your innovation into the heart of the European market?
- HealthTech founders
- Regulatory affairs and quality professionals
- Medical device innovators
- Digital health developers
- Consultants and innovation managers
Additional Information
For more information, please visit pathbootcamp.com
For any questions, please contact us at contact@pathbootcamp.com
Short Description
The Pathways for Regulatory and Market Access Bootcamp (PATH Bootcamp) is a 13-week training program that provides participants with a comprehensive overview of the complex European regulatory requirements for medical devices and in vitro diagnostic medical devices (IVDs).
Project Website
Project Description
The Pathways for Regulatory and Market Access Bootcamp (PATH Bootcamp) is a 13-week training program that provides participants with a comprehensive overview of the complex European regulatory requirements for medical devices and in vitro diagnostic medical devices (IVDs). The program combines live sessions, recorded learning content, interactive Q&A sessions, and practical exercises to impart both theoretical knowledge and practical skills. It is divided into three core modules: Regulatory Compliance, Early Health Technology Assessment (eHTA), and Market Access & Reimbursement Strategies.
Activities
- Introductory and Q&A sessions with experts on the following topics:
- Regulatory Compliance
- Early Health Technology Assessment (eHTA)
- Market Access and Reimbursement Strategies
- Personalized one-on-one mentoring tailored to participants’ needs
Goal
The goal of the program is to equip participants with the necessary skills and relevant expertise to navigate the European regulatory, market access, and health economics landscape for medical technologies with confidence.
Activities
- Introductory and Q&A sessions with experts on the following topics:
- Regulatory Compliance
- Early Health Technology Assessment (eHTA)
- Market Access and Reimbursement Strategies
- Personalized one-on-one mentoring tailored to participants’ needs
Goal
The goal of the program is to equip participants with the necessary skills and relevant expertise to navigate the European regulatory, market access, and health economics landscape for medical technologies with confidence.
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PROJECT TESTIMONIALS
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