Introduction to the New EU Medical Device Regulation (MDR) eLearning Course

Content Course

1. An overview of the new regulation
2. The key changes you need to be aware of
3. What EU MDR means in practice
4. Where you can find further information
5. A quiz to test your knowledge

1. This course is intended for, but not limited to, regulatory personnel, managers, CEO, CFO, or any medical device or IVD field personnel who want to learn about the new regulations.
2. The product we offer is a services and any disputes related to the services must be resolved directly with PT. SGS Indonesia.
3. All sales are final, and there will be no refunds provided for services purchased through our platform.
4. The SGS certificate is available to download once you have achieved a pass mark of 80% or more in the final assessment to complete this course.
5. The services purchased trough our platform are valid for 1 (one) year from the date of purchased.
6. The details on how to use or redeem the services will be provided in the order confirmation email sent to you upon successful purchase. Please carefully review this information, including any unique codes, instructions, or links provided.