Medical Device Design and Development for New and Legacy Products Training Course
Module 1 is Free to Attend – Register Below
Learn more about the course (dates, price, skills gained, and when module 1 is) by visiting the course page.
Module 1 Overview | Overview of the regulatory requirements and routes to market
Live and Recorded | 60 Minutes
Overview of the regulatory requirements and routes to market
- Regulatory pathways
- Overview of the Medical Device Regulation (MDR)
- EU vs US (FDA) – markets to consider
- Medical device vs combination product (drug/device and device/drug) – which regulation applies?
- Device classification and the implications for your product
Register for the free Module 1 by completing the form below. You will be sent joining instructions and more information about the course (agenda, trainers, pricing etc).