PATH Bootcamp

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.

• 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

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.